SHOWCASE COMING SOON Nu from the EXPERTS You Trust Obagi Has Extended Its Skincare Expertise

Supplement to July/August 2021

SHOWCASE COMING SOON Nu from the EXPERTS you trust Obagi has extended its skincare expertise

Obagi is about transformation, creating products that deliver results and empower conﬁdence. Our newest innovation expands on that promise.

YOU WON’T WANT TO MISS THIS

Continuous Outperforms A Higher Rate NEW TO OBAGI: Can’t wait for the Improvement* the Competition* of Results* revolutionary product?

Reach out to your local sales *2021 16-week double blinded study. Data on ﬁle at Obagi Cosmeceuticals LLC. All products/brand names, whether designated by notice or not ( /TM), are trademarks of Obagi Cosmeceuticals LLC and/or its afﬁliates. Distributed by Obagi Cosmeceuticals LLC. representative to learn more © 2021 Obagi Cosmeceuticals LLC. All rights reserved. COMING SOON Nu from the EXPERTS you trust Obagi has extended its skincare expertise

Obagi is about transformation, creating products that deliver results and empower conﬁdence. Our newest innovation expands on that promise.

YOU WON’T WANT TO MISS THIS

Continuous Outperforms A Higher Rate NEW TO OBAGI: Can’t wait for the Improvement* the Competition* of Results* revolutionary product?

Reach out to your local sales *2021 16-week double blinded study. Data on ﬁle at Obagi Cosmeceuticals LLC. All products/brand names, whether designated by notice or not ( /TM), are trademarks of Obagi Cosmeceuticals LLC and/or its afﬁliates. Distributed by Obagi Cosmeceuticals LLC. representative to learn more © 2021 Obagi Cosmeceuticals LLC. All rights reserved. Holden Timeless Beauty in San Diego. “Not only do clients have 30 percent less fat after the treatment, but they also build 25 percent more muscle mass in the area, which gives them more than other devices out there.”

Treatment typically consists of four sessions, spaced two to five days apart, over a two-week period. Research shows that the fat reduction and muscle stimulating results are maintained at six months.

Thanks to the radiofrequency heating, the muscle MORE IS LESS…FINALLY temperature quickly rises by several degrees to The phrase “less is more” is often bandied about. prepare muscles for stress. In less than four minutes, While this may be true and desirable in certain the temperature in the subcutaneous fat layer situations, when it comes to aesthetic outcomes reaches levels that cause apoptosis. HIFEM plus and return on investment, both patients and radiofrequency energy causes muscle contractions at providers want more for less. intensities that are not achievable during a workout. Extreme stress forces the muscle to adapt, resulting With the successful launch of EMSCULPT NEO, BTL in an increase in the number and growth of muscle is finally able to give them what they want: more fibers and cells. This is akin to doing about 24,000 fat loss and muscle toning in fewer treatments muscle contractions in 30 minutes. The combination (patients) and the ability to treat more patients in of HIFEM plus RF is stronger than when either Body fewer treatments (providers). Plus, these enhanced technology is used on its own, Dr. Holden notes. benefits come with lower costs to patients and in providers, compared to other interventions. “This saves time for the client and provides better Shaping efficacy,” she says. There’s no downtime, so EMSCULPT NEO is the only device that combines patients can go back to their lives as soon as the high-intensity, focused electromagnetic (HIFEM®) treatment is finished. energy and novel synchronized radiofrequency (RF) technology for simultaneous fat reduction and EMSCULPT NEO is also approved for body mass muscle stimulation. indexes (BMIs) of 35 or higher, which greatly expands the patient population. “In the past, patients “EMSCULPT NEO can achieve the holy grail of what who were also looking for fat reduction needed to we look for in body contouring: firmer buttocks, also use other energy-based devices and sometimes reduced layers of fat, and greater muscle definition,” minimally invasive surgeries to achieve what we can says New York City dermatologist Paul Jarrod Frank, now achieve with EMSCULPT NEO alone,” Dr. Frank EMSCULPTNEO.COM | #EMSCULPT MD, founder of PFRANKMD. EMSCULPT NEO can says. It’s also the only nonsurgical treatment that has treat the abdomen, buttocks, arms, and calves. been shown to be effective in treating abdominal separation, he adds. “In just four 30-minute sessions, clients get the most fat loss out of any device on the market,” says By strengthening the core and boosting muscle Amanda Holden, MD, owner and Medical Director at mass, EMSCULPT NEO also alleviates back Fat discomfort and helps patients get back to doing activities they once enjoyed, he says.

EMSCULPT NEO is cost-effective for patients and providers, he says. There are no consumables and fewer overhead costs (savings can be passed on to patients), and fewer hands are needed to administer the dual treatment, resulting in greater ROI in less time. Muscle 899-79EMCNFAAMAENUS100, Emsculpt_Neo_LF_FAA_9x10,75_ENUS100 899-79EMCNFAAMAENUS100,

Results As with any medical procedure, ask your doctor if the Emsculpt Neo® procedure is right for you. Emsculpt Neo® is intended for non-invasive lipolysis (breakdown of fat) of the abdomen and reduction in circumference of the abdomen with Skin Type I to Skin and patient Type III. Emsculpt Neo® is also cleared for improvement of abdominal tone, strengthening of the abdominal muscles and development of firmer abdomen. Strengthening, toning, firming of buttocks, thighs, and calves. Improvement of muscle tone and firmness, experience for strengthening muscles in arms. ©2020 BTL Group of Companies. All rights reserved. BTL® , EMSCULPT NEO® and EMSCULPT® are registered trademarks in the United States of America, the European Union, or other countries. The products, the methods of may vary. manufacture or the use may be subject to one or more U.S. or foreign patents or pending applications. Trademarks EMSCULPT®, EMSCULPT NEO®, EMSELLA®, EMTONE®, EMBODY®, and HIFEM® are parts of EM™ Family of products. *Data on file.

Emsculpt_Neo_LF_FAA_9x10,75_ENUS100.indd 1 16.10.2020 10:40:02 Untitled-1 1 12/15/20 9:21 AM

Body in Shaping

EMSCULPTNEO.COM | #EMSCULPT

Fat

Muscle 899-79EMCNFAAMAENUS100, Emsculpt_Neo_LF_FAA_9x10,75_ENUS100 899-79EMCNFAAMAENUS100,

Emsculpt_Neo_LF_FAA_9x10,75_ENUS100.indd 1 16.10.2020 10:40:02 Untitled-1 1 12/15/20 9:21 AM The Father of Barrier Repair “I created Epionce to help me be a better doctor.” — Dr. Carl R. Thornfeldt The Father of Barrier Repair “I created Epionce to help me be a better doctor.” — Dr. Carl R. Thornfeldt Now FDA-cleared to treat wrinkles of the neck! SKINPEN® PRECISION: The Highest Standard IN MICRONEEDLING TECHNOLOGY

The Engineering Superiority of SkinPen® Precision The Engineering Superiority of the Advanced Cartridge Unit SkinPen Precision is the first FDA-cleared microneedling device and only FDA-cleared microneedling procedure U.S. Patent Number 10,667,830 B2 that is U.S. engineered and manufactured and proven to be safe and effective through two clinical trials and over 90 validation studies. In addition, SkinPen Precision has differentiated features to enhance the provider Validated to maintain sharpness of needles for at least 80 minutes in experience and drive safety and results in patients. Validated to actively retract the use on on scar tissue, allowing you needles using our patented cartridge’s to safely treat larger areas with one reciprocating mechanism, which consumable cost, therefore driving ensures precise microchannels, higher revenue into your practice. Validated to maintain 7000 +/- rpm while providing a smooth glide (+/- 10%) with Intuitive Speed and optimal patient comfort. Control regardless of skin thickness, which ensures you get a predictable response for all patient types. Validated to penetrate to the depth Validated to prevent backflow from at wich the device is set, which cartridge to handpiece, reducing your allows you to be prescriptive in your LED smart technology ensures patients risk of cross contamination procedure and work at the precise 3 optimal performance for each and ensuring a safe treatment. depth needed for optimal results. 2 procedure meaning that you are 1 never treating a patient with a device that is not optimized.

Validated to maintain continuous power with a Lithium-Ion Rechargeable Battery, which means that whether your device is 100% charged or 10% charged, you are still offering your patients I like when a company goes out SkinPen Precision continues to set the standard for I value scientific studies, the same consistent procedure. “ of their way to show their results. the microneedling industry with their innovative that is why I use the only The recent clinical trial makes technology. As the only microneedling device FDA-cleared microneedling Ultrasonically Sealed Handpiece to prevent penetration of blood, SkinPen the first and only device FDA-cleared for both the face and neck, I am device for treating the face and fluid or serum, giving you peace with safe and effective results confident that I am providing my patients with the neck, SkinPen, in my practice. of mind that you are using a for both the face and the neck. safest, clinically proven treatment on the market. My patients deserve the best. device that is safe and effective. Worldwide distribution Dr. Jason Bloom Dr. Suneel Chilukuri Dr. Mary Lupo 30 in over 30 countries Cordless design utilizing Only microneedling device to conduct over 90 validation Inductive Charging to provide 90 studies to ensure quality, safety and performance* continuous power so that you Percentage of SkinPen Precision Customers never have to worry about losing that expressed high satisfaction*** 96 The SkinPen® Precision system is a microneedling device and accessories intended to be used as a battery power mid-procedure. treatment to improve the appearance of wrinkles of the neck for Fitzpatrick skin types II - IV and to ” Over 10,000 aesthetic practices worldwide are performing improve the appearance of facial acne scars in adults with all Fitzpatrick skin types aged 22 years and 10,000 life-changing SkinPen Precision procedures older. Rx only. *Data on file. **Crown Aesthetics Customer Satisfaction Survey March 2019 (data on file). For complete clinical trial summary and important safety information including contraindication and SkinPen Precision has been a trusted how to use the SkinPen Precision microneedling device, visit skinpen.com. 2 million+ microneedling choice for over 2 million patients ©2021 Crown Aesthetics | PN#LIT210603

SP_Magazine_Supplement_Spread_18x10.75_20210608.indd All Pages 6/9/21 12:03 PM Now FDA-cleared to treat wrinkles of the neck! SKINPEN® PRECISION: The Highest Standard IN MICRONEEDLING TECHNOLOGY

SP_Magazine_Supplement_Spread_18x10.75_20210608.indd All Pages 6/9/21 12:03 PM REVISION SKINCARE’S REVOX™ LINE RELAXER: An Innovation in Aesthetics Neuromodulator injections remain one of the most popular procedures in aesthetic practices, and the newest product from 45-Year-old Subject at Maximum Smile, Fitzpatrick Skin Type III Revision Skincare® can help enhance results. TOP: Revox™ Line Relaxer + Neuromodulator before (Pre-Injection) and 12 Weeks Post-Injection,4 Left Side BOTTOM: Placebo + Neuromodulator Before (Pre-Injection) and 12 Weeks Despite slight decreases in demand for some aesthetic procedures in 2020 Post-Injection, Right Side due to COVID-19 pandemic shutdowns, American Academy of Facial Plastic and Reconstructive Surgery members reported neuromodulator demand caused by dermal dehydration. The formulation contains Arnica Montana Flower Extract, 1 remained consistent with 2019 demand. And American Society of Plastic which soothes stressed skin and pairs well with neuromodulators. Surgeons members cited a significant uptick in demand during the pandemic, with current patients eager to reschedule missed neurotoxin and filler A SYNERGISTIC PAIRING appointments and new patients motivated for the first time to pursue the Use of Revox Line Relaxer with a neuromodulator in a multi-center double-blind, split- 2 minimally invasive facial treatments. Aesthetic physicians expect demand to face, placebo-controlled study demonstrated variable results with several key clinical continue to rise as people become vaccinated and the country reopens. parameters at rest and maximum expression after 12 weeks of twice daily use.4

Board-certified dermatologist Corey L. Hartman, MD, Founder of Skin Wellness Revox Line Relaxer is well tolerated and can be used immediately post-neuromodulator Dermatology in Birmingham, AL (instagram.com/dr.coreyhartman), says his neu- injection.4 Its unique applicator allows for precise, targeted use while delivering a sooth- romodulator business is through the roof, noting a boom in millennial patients ing, cooling effect. seeking prejuvenation treatments now in hopes of preventing the need for heavy-duty procedures down the line. He’s excited about a new product from Re- In addition to creating a powerful synergy when used in conjunction with a neuromodulator, vision Skincare that can help optimize the benefits of neuromodulator injections. when Revox™ Line Relaxer was used as a stand-alone product during a 12-week clinical study, the results were also impressive. Fifteen minutes post-application, 97 percent of subjects Revision Skincare has once again pushed the boundaries of topical product showed a highly statistically significant improvement in expression lines and under-eye lines, performance by creating Revox™ Line Relaxer, an advanced targeted serum and 45 percent of subjects showed a highly statistically significant improvement in wrinkles.5 specifically designed to be paired with a neuromodulator. This clinically-prov- After eight weeks, subjects showed a 29 percent average reduction in expression lines and en formula features LineRelax™ Technology that works synergistically with under-eye lines, which increased to a 38 percent average reduction after 12 weeks.5 There neuromodulator injections AND for extending beyond general injection areas was also a highly statistically significant improvement in radiance, visual texture, and overall to deliver the best of both worlds for dramatic, natural-looking results. appearance.5 In fact, significant benefits were seen in the periorbital area when measured by 3D PRIMOSCR (Canfield Scientific, Parsippany, NJ). After 12 weeks, subjects showed a statisti- AN INNOVATIVE LINE RELAXER cally significant reduction in total wrinkle length and area in the periorbital area.6 Revox Line Relaxer’s patent-pending LineRelax Technology not only reduces the intensity of expression lines by inhibiting acetylcholine release from the RESULTS YOU CAN SEE: QUALITY SKIN nerve ending to the muscle, but also works at the epidermal level mitigat- No one thing can give skin everything that it needs. And that’s why a synergistic ing the release of acetylcholine from the keratinocyte and dissemination skincare solution combining the benefits of neuromodulator injections and a topical throughout the facial skin. An in vitro study using a full-thickness tissue product like Revox™ Line Relaxer is the answer. model to measure acetylcholine release at the epidermal level, found that tissue treated with Revox Line Relaxer had a 37 percent reduction of acetyl- “We’ve become so neuromodulator dominant that we think they can do everything, choline at 72 hours (p<0.05) and a 49.9 percent reduction of acetylcholine but the relaxation of the muscles can only do so much. Remember, people cannot see 3 at 96 hours (p<0.01) when compared to untreated (negative control). your neuromodulator or your fillers. What people see is the quality of your skin. Revox™ Line Relaxer not only enhances the results of neuromodulators, but it also rejuvenates To optimize the benefits of neuromodulator injections, this proprietary the health of the skin over time, which neuromodulators cannot do,” says Shino Bay technology is powered by five neuromodulating bioavailable peptides plus Aguilera, DO, a board-certified dermatologist in practice in Fort Lauderdale, FL. Gamma-Aminobutyric Acid (GABA) to reduce horizontal and vertical expression lines including forehead and glabellar lines, crow’s feet and under-eye *Vehicle control represents neuromodulator + placebo serum lines, nasolabial folds, marionette and vertical lip lines. Revox Line Relaxer provides essential benefits that can significantly improve overall skin ap- 1. https://www.aafprs.org/Media/Press_Releases/PageTemplates/New%20Survey%20Results%20Announced%20Feb.%201,%202021.aspx 2. https://www.plasticsurgery.org/news/press-releases/american-society-of-plastic-surgeons-unveils-covid19s-impact-and-pent-up-patient-demand-fueling-the-industrys-current-post-pandemic-boom pearance, skin radiance, and visual and tactile texture. It is formulated with 3. Alisar S. Zahr, John Koch, Thu Q. Nguyen, Tatiana Kononov. A Novel Blend of Neuromodulating Peptides and Gamma Aminobutyric Acid to Regulate the Release of Acetylcholine. Annual Meeting of the American Academy of Dermatology. VMX 2021. April 23-25, 2021. a Dermal Support Blend of three bioavailable reparative peptides plus two 4. Manuscript in preparation. 12-week procedure-pairing study. Data on file. Results may vary. 5. Nguyen, TQ; Zahr, AZ; Kononov, T; Ablon, G. A Randomized, Double-Blind, Placebo-Controlled Clinical Study Investigating the Efficacy and Tolerability of a Peptide Serum Targeting Expression Lines. Journal of highly efficacious botanical extracts to help reduce fine lines and wrinkles Clinical and Aesthetic Dermatology. May 2021. Accepted. Results may vary. and improve skin elasticity. Plus hyaluronic acid and inulin, a prebiotic, work 6. 3D PRIMOSCR Imaging (Canfield Scientific, Parsippany, NJ) clinical images were taken at the bilateral region of the face of both left and right side under standard light and robust high pass filter. Based on results from a clinical study on 55 women, ages 35-60, after 12 weeks of twice-daily use. Data on file. Results may vary. synergistically to hydrate skin to improve the look of fine lines and wrinkles

Your Complete Body BY TRUSCULPT Sculpting Solution A body sculpting solution to reduce fat1,2 and build muscle3 with two innovative technologies. By pairing the truSculpt® iD and truSculpt® flex devices, truBody delivers a personalized PERSONALIZED EXPERIENCE treatment experience with long-lasting results, high patient • Fully customizable based on patient goals satisfaction and an average of 24% reduction in fat.1,2 • Treat all body and skin types and all fitness levels with no BMI restrictions • Comfortable with no downtime

15 MINUTE TREATMENT TREAT MORE AREAS EFFECTIVE TREATMENTS • Increase muscle mass and reduce with an average of treat 8 areas at once to subcutaneous fat 1,2 • Target specific areas that need more 24% TONE definition Customizable treatments FAT REDUCTION1,2 FIRM & STRENGTHEN •

MAXIMUM ROI • Quick treatments to increase throughput • Low cost of consumables • High patient satisfaction • Growing market segment Photos Courtesy of A. Moradzadeh, M.D. of A. Moradzadeh, Courtesy Photos Before After 4 Weeks 1 truSculpt iD Tx & 4 truSculpt flex Tx Sculpt a stronger practice with truBody by Cutera Learn more at cutera.co/trytrubody Photos Courtesy of River Aesthetics of River Courtesy Photos

Before After 4 Weeks 1 Taub A, Bartholomeusz J. Ultrasound Evaluation of a Single Treatment With a Temperature 1 truSculpt iD Tx & 5 truSculpt flex Tx Controlled Multi-Frequency Monopolar Radio Frequency Device for the Improvement of Localized Adiposity on the Abdomen and Flanks. J Drugs Dermatol. 2020;19(1):28-34 2 Somenek MT, Ronan SJ, Pittman TA. A Multi-Site, Single-Blinded, Prospective Pilot Clinical Trial for Non-Invasive Fat Reduction of the Abdomen and Flanks Using a Monopolar 2 MHz Radiofrequency Device. Lasers Surg Med. 2021 Mar;53(3):337-343 3 Stephen J. Ronan M.D. A Novel Bio-Electric Current Stimulation Device For Improvement Of © 2021 Cutera, Inc. All rights reserved. AP003670 rA (07/21) Muscle Tone 7/2019.

Modern Aesthetics_Innovation Supplement_V2.indd 1 8/3/21 10:10 AM Your Complete Body BY TRUSCULPT Sculpting Solution A body sculpting solution to reduce fat1,2 and build muscle3 with two innovative technologies. By pairing the truSculpt® iD and truSculpt® flex devices, truBody delivers a personalized PERSONALIZED EXPERIENCE treatment experience with long-lasting results, high patient • Fully customizable based on patient goals satisfaction and an average of 24% reduction in fat.1,2 • Treat all body and skin types and all fitness levels with no BMI restrictions • Comfortable with no downtime

Modern Aesthetics_Innovation Supplement_V2.indd 1 8/3/21 10:10 AM THE AGE-DEFYING POWERHOUSE

As skin ages, its rejuvenative processes perform less efficiently. One key reason is a lack of cellular communication, which can accelerate the loss of collagen and impair skin elasticity. At SkinMedica®, we are the industry leader in skin rejuvenation because we target one of the primary causes of visible skin aging—diminishing growth factors.

We took it to the next level with TNS® Advanced+ Serum—the only growth factor product proven to address sagging skin. It significantly smooths the appearance of coarse wrinkles and fine lines, with results in as little as 2 weeks and progressive results over 24 weeks.1

IN CLINICAL STUDIES 1:

6Y +

6 YEARS YOUNGER APPEARANCE OF PROGRESSIVE A third-party, validated psychometric scale SAGGING SKIN IMPROVEMENT revealed that patients felt they looked up Significant improvements in the appearance Subjects felt increasingly more satisfied with THE GROWTH to 6 years younger after 12 weeks. of sagging skin after 8 weeks. continued use measured over 24 weeks. PATIENTS SAW DRAMATIC RESULTS FACTOR 1 VISIBLE RESULTS KEEP GETTING BETTER, WITH PROGRESSIVE IMPROVEMENT.

AUTHORITY IMPROVEMENTS AT WEEK 2 IMPROVEMENTS AT WEEK 24 TNS® ADVANCED+ SERUM SKINMEDICA® DELIVERS OUR MOST ADVANCED GROWTH FACTOR TECHNOLOGY.

+ The only growth factor product proven to address sagging skin1 + Smooths the appearance of coarse wrinkles and fine lines + Results starting in just 2 weeks1 + Progressive results, even at 24 weeks1

+ BASELINE + 2 WEEKS + BASELINE + 24 WEEKS

Female, age 60, Fitzpatrick Skin Type II. Unretouched photos, taken in standard lighting. Female, age 68, Fitzpatrick Skin Type II. Unretouched photos, taken in standard lighting. Individual results may vary. Individual results may vary.

With TNS® Advanced+ Serum, SkinMedica® goes further than ever in addressing the visible signs of skin aging.

VISIT SKINMEDICA.COM/TNSADVANCEDPLUS TO LEARN MORE.

1. Data on file at SkinMedica®. The SkinMedica® product described here is intended to meet the FDA’s definition of a cosmetic product, an article applied to the human body to cleanse, beautify, promote attractiveness, and alter appearances. This SkinMedica® product is not intended to be a drug product that diagnoses, treats, cures, or prevents any disease or condition. This product has not been approved by the FDA, and the statements here have not been evaluated by the FDA.

011871 TNSA+ModernAesthetics_ST.indd 1 6/10/21 1:02 PM THE AGE-DEFYING POWERHOUSE

IN CLINICAL STUDIES 1:

6Y +

AUTHORITY IMPROVEMENTS AT WEEK 2 IMPROVEMENTS AT WEEK 24 TNS® ADVANCED+ SERUM SKINMEDICA® DELIVERS OUR MOST ADVANCED GROWTH FACTOR TECHNOLOGY.

+ BASELINE + 2 WEEKS + BASELINE + 24 WEEKS

With TNS® Advanced+ Serum, SkinMedica® goes further than ever in addressing the visible signs of skin aging.

VISIT SKINMEDICA.COM/TNSADVANCEDPLUS TO LEARN MORE.

011871 TNSA+ModernAesthetics_ST.indd 1 6/10/21 1:02 PM Sponsored By ANNUAL, MONTHLY, DAILY RENTAL PROGRAMS AVAILABLE Sensus Healthcare has recently partnered with Sentinel, a cloud-based asset-management, remote monitoring and diagnostic platform. Sentinel is a cloud platform installed directly onto any Sensus laser to provide real- time information about the status of your system.

Sentinel™ Cloud Features keloids, non-melanoma skin cancer, and cosmetic Sensus Body Contouring The Sentinel™ cloud system has several features concerns. Our aesthetic lasers now present The Sensus Body Contouring is a non-invasive laser to keep your systems at your practice on track. dermatology providers the opportunity to offer their treatment that destroys fat cells with hyperthermia The platform boasts continuous remote monitoring patients more ways to treat pigmentation, wrinkles, technology. Results are seen as quickly as six to track the status of your system from any web unwanted hair or tattoos, body contouring, and weeks, and optimal fat loss results are usually seen browser or iOS device. Continuous backups ensure more. in 12 weeks. that valuable information is safely stored in the cloud, and allows providers with multiple locations Sensus Q-Switch Sensus CO2 or group practices can monitor remotely at all times. The Sensus Q-Switch is used for tattoo removal and As the most used laser in the dermatology field, the The Sentinel™ system also allows providers to to treat unwanted dark spots. Sensus CO2 treats scars, fine lines, wrinkles, and monitor any service issues without having to send an While this laser treats pigmented skin, moles, and age spots. The CO2 laser is ideal for skin treatments engineer to the field, such as calibration, monitoring freckles, it is also used for tattoo removal. This because of the skin’s high water percentage. Over voltage and temperature. laser is best for darker-colored tattoos, as lighter the past few years, advances in laser technology colors such as green and yellow tattoo ink might not have allowed cosmetic surgeons to provide Each practice has customizable access to the benefit as much. their clients with the best solutions. Traditional Sentinel™ data. You can use a single physician login, treatments are being replaced with laser treatments or allow multiple users to access data by simply Sensus PICO for the correction of scars and wrinkles. The range downloading the app and signing on from a unique The Sensus PICO treats age spots, freckles, of uses for the CO2 laser is expected to continue to login. All data on Sentinel™ adheres to HIPAA pigmented lesions, fine lines, wrinkles, acne scars, grow in the future! regulations and is safely stored. From the moment and removes tattoos. The rapid energy delivery you switch the device on, everything is being from the picosecond laser technology prevents heat monitored for compliance. These compliance reports from building up, eliminating side effects such as can be tailored to each practice’s needs, such as blistering or burns. A majority of patients experience If you are a healthcare tracing records, patient information, or switching a safe and effective treatment with reduced side professional in the South information to Physicists Only or Service Only. effects. Picosecond laser technology was originally used for tattoo removal, but studies have shown Florida area interested in Sentinel™ makes it easy to store patient information this laser to be effective for other dermatology renting the Sensus Aesthetic and manage assets. It can easily track your patient’s treatments, reducing the number of treatments information, including prescriptions and visits. With needed. Lasers, contact us today! Sentinel in place, you will never have to worry about losing your patient data or experiencing Sensus IPL Call 561.922.5808 or visit prolonged downtimes. The Sensus IPL technology is used by medical professionals to perform a variety of skin Sensushealthcare.com to The Five Sensus Smart Lasers treatments, including hair removal. The procedure learn more about our services. At Sensus Healthcare, Inc., we specialize in usually spans about 25 to 30 minutes but depends effective treatments for both oncological and non- on the area treated. Patients will have an average of oncological conditions. We offer several medical four to six weeks gap between procedures. There is devices and laser systems to treat a variety of little to no downtime for recovery. Sponsored By ANNUAL, MONTHLY, DAILY RENTAL PROGRAMS AVAILABLE Sensus Healthcare has recently partnered with Sentinel, a cloud-based asset-management, remote monitoring and diagnostic platform. Sentinel is a cloud platform installed directly onto any Sensus laser to provide real- time information about the status of your system. Annual, Monthly, Daily Rental programs available Are you a healthcare professional? Would you like an easy way to offer in-office aesthetic lasers procedures without Sentinel™ Cloud Features keloids, non-melanoma skin cancer, and cosmetic Sensus Body Contouring the hassle that comes with equipment ownership in-office? The Sentinel™ cloud system has several features concerns. Our aesthetic lasers now present The Sensus Body Contouring is a non-invasive laser to keep your systems at your practice on track. dermatology providers the opportunity to offer their treatment that destroys fat cells with hyperthermia patients more ways to treat pigmentation, wrinkles, The platform boasts continuous remote monitoring technology. Results are seen as quickly as six We Offer to track the status of your system from any web unwanted hair or tattoos, body contouring, and weeks, and optimal fat loss results are usually seen browser or iOS device. Continuous backups ensure more. in 12 weeks. No long-term Comprehensive laser that valuable information is safely stored in the financial commitment training and support cloud, and allows providers with multiple locations Sensus Q-Switch Sensus CO2 No obsolescence concerns associated Customize in-service or group practices can monitor remotely at all times. The Sensus Q-Switch is used for tattoo removal and As the most used laser in the dermatology field, the with equipment ownership Supplemental Lead to treat unwanted dark spots. The Sentinel™ system also allows providers to Sensus CO2 treats scars, fine lines, wrinkles, and Delivery & Pick Up Generation monitor any service issues without having to send an While this laser treats pigmented skin, moles, and age spots. The CO2 laser is ideal for skin treatments engineer to the field, such as calibration, monitoring freckles, it is also used for tattoo removal. This because of the skin’s high water percentage. Over voltage and temperature. laser is best for darker-colored tattoos, as lighter the past few years, advances in laser technology colors such as green and yellow tattoo ink might not have allowed cosmetic surgeons to provide Monthly Each practice has customizable access to the benefit as much. their clients with the best solutions. Traditional Sentinel™ data. You can use a single physician login, treatments are being replaced with laser treatments Q-switch Pico IPL CO2 Body or allow multiple users to access data by simply Sensus PICO for the correction of scars and wrinkles. The range •Pigmentation •Age Spots, Freckles, •Hair Removal •Scars, Fine Lines, Contouring downloading the app and signing on from a unique The Sensus PICO treats age spots, freckles, of uses for the CO2 laser is expected to continue to •Tattoo Removal Pigmented Lesions •Dark Spots and Wrinkles •Fat Reduction login. All data on Sentinel™ adheres to HIPAA pigmented lesions, fine lines, wrinkles, acne scars, grow in the future! •Fine Lines and Wrinkles Wrinkles •Age Spots regulations and is safely stored. From the moment and removes tattoos. The rapid energy delivery •Acne Scars •Tattoo Removal you switch the device on, everything is being from the picosecond laser technology prevents heat monitored for compliance. These compliance reports from building up, eliminating side effects such as can be tailored to each practice’s needs, such as blistering or burns. A majority of patients experience If you are a healthcare tracing records, patient information, or switching a safe and effective treatment with reduced side professional in the South information to Physicists Only or Service Only. effects. Picosecond laser technology was originally used for tattoo removal, but studies have shown Florida area interested in Sentinel™ makes it easy to store patient information this laser to be effective for other dermatology renting the Sensus Aesthetic and manage assets. It can easily track your patient’s treatments, reducing the number of treatments information, including prescriptions and visits. With needed. Lasers, contact us today! Sentinel in place, you will never have to worry about losing your patient data or experiencing Sensus IPL Call 561.922.5808 or visit Hourly/Daily rentals prolonged downtimes. The Sensus IPL technology is used by medical professionals to perform a variety of skin Sensushealthcare.com to also available for: The Five Sensus Smart Lasers treatments, including hair removal. The procedure learn more about our services. At Sensus Healthcare, Inc., we specialize in usually spans about 25 to 30 minutes but depends •Resurfacing •Tattoo Removal effective treatments for both oncological and non- on the area treated. Patients will have an average of •Hair Removal •Pigmentation oncological conditions. We offer several medical four to six weeks gap between procedures. There is devices and laser systems to treat a variety of little to no downtime for recovery.

For more information visit Fully Customizable Options Available SensusHealthcare.com or call us today 407.963.4833 BEFORE AFTER

WHY IS DYSPORT JUST RIGHT FOR YOUR AESTHETIC PATIENTS RIGHT NOW?

There’s no doubt our world is changing, as technology revolutionizes the ways we present—and see— ourselves. From the ubiquitous selfie to hours spent using videoconferencing technology, women and men see themselves in new and different ways. And many Frown before (left) and after 50 units Dysport, Day 27 (right). Actual patient. Individual results may vary. want to improve what they see. But the “Zoom Boom” The most common side effects are nose and throat irritation, headache, injection site pain, injection site skin and “Selfie-awareness” driving demand for aesthetic reaction, upper respiratory tract infection, eyelid swelling, eyelid drooping, sinus inflammation and nausea. interventions are just the headline to the story. What really matters is that aesthetic providers deliver on the promise of a rejuvenated, natural-looking appearance,1 with more than half of all subjects seeing improvement in just two to so that patients are satisfied* with the face they see in snaps, grams, and three days after injection.†,1,4-6 teleconference screens for months to come. The implications for patient care are significant. Aesthetic injectors who Enter Dysport® (abobotulinumtoxinA) for injection* from Galderma. reach for Dysport offer patients a fast-acting,† long-lasting* effect on Dysport is an acetylcholine release inhibitor and a neuromuscular wrinkles between the brows, so that wherever they see themselves, they blocking agent indicated for the temporary improvement in the will see an aesthetic benefit.1,4-6 appearance of moderate to severe glabellar lines associated with procerus and corrugator muscle activity in adults <65 years of age. Dysport is trusted by patients and providers, being shown safe in more Clinical research demonstrates that Dysport can provide long lasting, than 3,120 study participants and over 12 years of approved use in the natural-looking effects to support patient satisfaction.*,1 In fact, in a US.3,7-9 Plus, abobotulinumtoxinA has more than 25 years of clinical recent study, 97 percent of subjects receiving Dysport said they thought experience worldwide for therapeutic and aesthetic uses.10 Galderma also their results looked natural six months after treatment.1 offers training and support for injectors, and patients enjoy the benefits of a market-leading loyalty program.

BURGEONING OPPORTUNITY THE TIME IS RIGHT More and more patients are embracing medical cosmetic treatments, turning to aesthetic injectables at the first signs of aging to maintain their A growing number of Americans—from aesthetic treatment novices to youthful appearance and achieve natural results. One recent consensus cosmetic experts—feel that now is the time to pursue aesthetic injectable report noted that among patients receiving facial aesthetic treatments treatment. The data and years of experience suggest that Dysport is just there is growing diversity with respect to age, gender, and ethnicity.2 right for this moment and moments come.

*Subject-reported at 12 months (N=120) after two treatments six months apart in a phase IV, multicenter, prospective study. With a large potential market to be tapped, successful cosmetic †A secondary endpoint based on Kaplan-Meier estimates of cumulative rate of time to onset of response. The median time to onset of surgeons focus on nurturing long-term relationships based on trust and response was 3 days in GL-1 (Dysport 55/105 [52%], placebo 3/53 [6%]) and GL-2 (Dysport 36/71 [51%], placebo 9/71 [13%]), and 2 days in GL-3 (Dysport 110/200 [55%], placebo 4/100 [4%]). patient satisfaction. After all, dissatisfied first-time patients often are one-time patients. 1. Dermatol Surg. 2021 Apr 1;47(4):504-509. 2. J Drugs Dermatol. 2020 Apr 1;19(4):s5-15. 3. Dysport. Prescribing Information. Fort Worth, TX: Galderma Laboratories, L.P., 2020. Evidence shows that Dysport supports high patient satisfaction.1 In 4. Data on file. MA-Y-97-52120-085 (GL-2) Clinical Study Report. Fort Worth, TX: Galderma Laboratories, L.P., 2007. 5. Data on file. GL-Y-97-52120-719 (GL-1) Clinical Study Report. Fort Worth, TX: Galderma Laboratories, L.P., 2007. an open-label, multicenter, interventional study that evaluated subject 6. Data on file. GL-Y-97-52120-718 (GL-3) Clinical Study Report. Fort Worth, TX: Galderma Laboratories, L.P., 2007. satisfaction following injections of abobotulinumtoxinA 50 U in the 7. Data on file . MA-41196. Fort Worth, TX: Galderma Laboratories, L.P., June 2019. 8. Data on File. 43USD1802 Clinical Study Report. Fort Worth, TX: Galderma Laboratories, L.P., 2020. glabellar lines at baseline and six months, 95 percent of subjects were 9. Data on File. 43USD1801 Clinical Study Report. Fort Worth, TX: Galderma Laboratories, L.P., 2020. satisfied with two treatments per year.1 Of note, treatment was fast-acting 10. http://www.mhra.gov.uk/home/groups/par/documents/websiteresources/con108644.pdf. Accessed December 6, 2019

Dysport® (abobotulinumtoxinA) for Injection is an acetylcholine release inhibitor have been reported at doses comparable to or lower than the maximum ADVERSE REACTIONS and a neuromuscular blocking agent indicated for the temporary improvement in recommended total dose. • In clinical studies, the most frequently reported adverse events (2%) were nasophar- the appearance of moderate to severe glabellar lines associated with procerus and yngitis, headache, injection site pain, injection site reaction, upper respiratory tract corrugator muscle activity in adults < 65 years of age. CONTRADICTIONS infection, eyelid edema, eyelid ptosis, sinusitis, nausea, and blood present in urine. • Hypersensitivity to any botulinum toxin product or excipients IMPORTANT SAFETY INFORMATION DISTANT SPREAD OF TOXIN EFFECT • Allergy to cow’s milk protein DRUG INTERACTIONS Postmarketing reports indicate that the effects of Dysport and all botulinum • Infection at the proposed injection site(s) • Concomitant use of Dysport and aminoglycosides or other agents interfering with toxin products may spread from the area of injection to produce symptoms neuromuscular transmission or muscle relaxants, should be observed closely consistent with botulinum toxin effects. These may include asthenia, WARNINGS AND PRECAUTIONS because effect of Dysport may be potentiated. generalized muscle weakness, diplopia, blurred vision, ptosis, dysphagia, • The potency Units of Dysport are not interchangeable with other preparations of • Anticholinergic drugs may potentiate systemic anticholinergic effects. dysphonia, dysarthria, urinary incontinence and breathing difficulties. botulinum toxin products and, therefore, units of biological activity of Dysport can- • The effect of administering different botulinum neurotoxins during course of These symptoms have been reported hours to weeks after injection. Swal- not be compared to or converted into units of any other botulinum toxin products. treatment with Dysport is unknown. lowing and breathing difficulties can be life threatening and there have • Immediate medical attention may be required in cases of respiratory, speech or been reports of death. The risk of symptoms is probably greatest in chil- swallowing difficulties, or serious hypersensitivity reactions. USE IN SPECIFIC POPULATIONS dren treated for spasticity but symptoms can also occur in adults treated • Recommended dose and frequency of administration should not be exceeded. • Dysport is not recommended for use in children or pregnant women. for spasticity and other conditions, particularly in those patients who have • Dry eye may occur with glabellar line treatment, if symptoms persist, consider underlying conditions that would predispose them to these symptoms. In referring patient to an ophthalmologist. You are encouraged to report negative side effects of prescription drugs to the FDA. unapproved uses and in approved indications, cases of spread of effect • Concomitant neuromuscular disorder may exacerbate clinical effects of treatment. Visit www.fda.gov/medwatch or call 1-800-FDA-1088. 9" W x 10.75" H

Actual patients. Individual results may vary.

You can have confidence that Dysport will deliver. Dysport® is a prescription injection for temporary improvement in the look of moderate to severe frown lines between the eyebrows (glabellar lines) in adults less than 65 years of age. HIGHLY SATISFIED PATIENTS 97% of users§ thought their results looked natural 6 months after treatment(1,†) FAST ACTING RESULTS Users§ see results in 2-3 days(2-4,*)

LONG LASTING RESULTS 95% of users§ were satisfied with just 2 Dysport Follow us on Instagram! treatments per year(1,†) @DysportUSA

§ Users= clinical trial subjects. Tell your doctor about all of your medical conditions, including if you have surgical changes to your face, very weak muscles in the treatment area, any abnormal facial change, injection site inflammation, droopy * A secondary endpoint based on Kaplan-Meier estimates of cumulative rate of time to onset of response. eyelids or sagging eyelid folds, deep facial scars, thick oily skin, wrinkles that can’t be smoothed by spreading The median time to onset of response was 3 days in GL-1 (Dysport 55/105 [52%], Placebo 3/53 [6%] and them apart, or if you are pregnant or breastfeeding or planning to become pregnant or breastfeed. GL-2 (Dysport 36/71 [51%], Placebo 9/71 [13%]), and 2 days in GL-3 (Dysport 110/200 [55%], Placebo 4/100 [4%]). Tell your doctor about all the medicines you take, including prescription and nonprescription medicines, vitamins and herbal and other natural products. Using Dysport with certain other medicines may cause † Subject-reported at 12 months (N=120) after two treatments six months apart in a phase IV, mulitcenter, serious side effects. Do not start any new medicines while taking Dysport without talking to your doctor prospective study. first. Indication Especially tell your doctor if you: have received any other botulinum toxin product, such as Myobloc® Dysport® (abobotulinumtoxinA) is a prescription injection for temporary improvement in the look of (rimabotulinumtoxinB), Botox® (onabotulinumtoxinA), or Xeomin® (incobotulinumtoxinA), in the last four moderate to severe frown lines between the eyebrows (glabellar lines) in adults less than 65 years of age. months or any in the past (be sure your doctor knows exactly which product you received, have recently received an antibiotic by injection, take muscle relaxants, take an allergy or cold medicine, or take a sleep Important Safety Information medicine. What is the most important information you should know about Dysport? Spread of Toxin Effects: In Common Side Effects some cases, the effects of Dysport and all botulinum toxin products may affect areas of the body away from the injection site. Symptoms can happen hours to weeks after injection and may include swallowing The most common side effects are nose and throat irritation, headache, injection site pain, injection site skin and breathing problems, loss of strength and muscle weakness all over the body, double vision, blurred reaction, upper respiratory tract infection, eyelid swelling, eyelid drooping, sinus inflammation, and nausea. vision and drooping eyelids, hoarseness or change or loss of voice, trouble saying words clearly, or loss of Ask your doctor if Dysport is right for you. bladder control. Swallowing and breathing problems can be life threatening and there have been reports of death. You are at the highest risk if these problems are pre-existing before injection. You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088. These effects could make it unsafe for you to drive a car, operate machinery, or do other dangerous activities. Please see Dysport Full Prescribing Information including Medication Guide at DysportUSA.com. Do not have Dysport treatment if you: are allergic to Dysport or any of its ingredients (see the end of the REFERENCES: Medication Guide for a list of ingredients), are allergic to cow’s milk protein, had an allergic reaction to any other botulinum toxin product, such as Myobloc®, Botox®, or Xeomin®, have a skin infection at the planned 1. Data on file. 43USD1802 Clinical Study Report. Fort Worth, TX: Galderma Laboratories, L.P., 2020.2. Data injection site, under 18 years of age, or are pregnant or breastfeeding. on file. MA-Y-97-52120-085 (GL-2) Clinical Study Report. Fort Worth, TX: Galderma Laboratories, L.P., 2007 3. Data on file. GL-Y-97-52120-719 (GL-1) Clinical Study Report. Fort Worth, TX: Galderma Laboratories, The dose of Dysport is not the same as the dose of any other botulinum toxin product and cannot be L.P., 2007. 4. Data on file. GL-Y-97-52120-718 (GL-3) Clinical Study Report. Fort Worth, TX: Galderma compared to the dose of any other product you may have used. Laboratories, L.P., 2007. Tell your doctor about any swallowing or breathing difficulties and all your muscle or nerve conditions © 2021 Galderma Laboratories, L.P. such as amyotrophic lateral sclerosis [ALS or Lou Gehrig’s disease], myasthenia gravis, or Lambert-Eaton The Dysport trademark is used under license. syndrome, which may increase the risk of serious side effects including difficulty swallowing and difficulty All trademarks are the property of their respective owners. breathing. Serious allergic reactions have occurred with the use of Dysport. Dry eye has also been reported. US-DYS-2100199 Emepelle, featuring MEP Technology®, is extensively studied and clinically proven* to help improve, LOVE hydration, firmness, luminosity, fine lines & wrinkles brought on by Estrogen Deficient Skin (EDS), non-hormonally. VISIBLE IMPROVEMENT WITHIN 8 WEEKS OF USE YOUR SKIN, MEP Technology is the only FEMALE, AGE 60 Non-hormonal Estrogen Receptor Aide (NERA) clinically proven to address the root cause REDEFINE The time to start considering Emepelle is of accelerated collagen loss and not when somebody is in menopause, skin aging brought on by EDS. where they’re losing 30 percent of their collagen in the first five years. I think the HOW IT AGES time to start considering Emepelle would Estrogen Deficiency is the cause * really be when people are having peri- of up to 30% collagen loss in the Baseline 8 Weeks menopausal symptoms and before they Emepelle is the only skincare line featuring have such a sharp drop-off. first five years of menopause and Unretouched photographs of patients at baseline and after ® 2.1% per year, thereafter. morning use of Emepelle Serum and evening use of Emepelle MEP TECHNOLOGY clinically proven* Night Cream. Individual results may vary. – Joel L. Cohen, MD, FAAD to help address the root cause of accelerated Photos courtesy of Joel L. Cohen, MD. collagen loss and skin aging due to ESTROGEN What I found most impressive in the study by Dr. Draelos were the biopsies DEFICIENT SKIN, non-hormonally. showing the re-emergence of estrogen receptors on fibroblasts that had been dormant for years after menopause following application of MEP.

– Diane Berson, MD, FAAD

Blinded investigator-assessedMEP EXTENSIVELY % improvement STUDIED AND after CLINICALLY 14 weeks’ application PROVEN MEP* vs vehicle

VISUAL CRITERIA MEP + VEHICLE PLACEBO P VALUE Rich. Firming. Rejuvenating. ASSESSMENT (% IMPROVEMENT) (% IMPROVEMENT)  54% 16% P<0.001 This rich, creamy, fast-absorbing eye cream helps reduce  39% 8% P<0.001 the appearance of fine lines and wrinkles, under-eye puffiness and dark circles for improved luminosity and  20% 2% P<0.001 anti-aging benefits for the delicate eye area.  19% 6% P<0.001

 11%   P=0.001

FEATURING:  9%   P<0.001 Innovative MEP Technology • Powerful antioxidants •   8% 2% P=0.001 Caffeine • Peptides • Hyaluronic acid • Emollients          . Blinded investigator-assessed % improvement after 14 weeks1 application MEP vs vehicle. Clinical Study conducted by Zoe Diana Draelos, MD and published in the JDD November, 2018 Dermatologist-tested • Ophthalmologist tested • Non-Irritating • Fragrance-Free For more information, please contact Customer Service at 1-866-424-6735 or [email protected] Emepelle is brought to you by Biopelle, a division of Ferndale Pharma Group.

*data on file Emepelle, featuring MEP Technology®, is extensively studied and clinically proven* to help improve, LOVE hydration, firmness, luminosity, fine lines & wrinkles brought on by Estrogen Deficient Skin (EDS), non-hormonally. VISIBLE IMPROVEMENT WITHIN 8 WEEKS OF USE YOUR SKIN, MEP Technology is the only FEMALE, AGE 60 Non-hormonal Estrogen Receptor Aide (NERA) clinically proven to address the root cause REDEFINE The time to start considering Emepelle is of accelerated collagen loss and not when somebody is in menopause, skin aging brought on by EDS. where they’re losing 30 percent of their collagen in the first five years. I think the HOW IT AGES time to start considering Emepelle would Estrogen Deficiency is the cause * really be when people are having peri- of up to 30% collagen loss in the Baseline 8 Weeks menopausal symptoms and before they Emepelle is the only skincare line featuring have such a sharp drop-off. first five years of menopause and Unretouched photographs of patients at baseline and after ® 2.1% per year, thereafter. morning use of Emepelle Serum and evening use of Emepelle MEP TECHNOLOGY clinically proven* Night Cream. Individual results may vary. – Joel L. Cohen, MD, FAAD to help address the root cause of accelerated Photos courtesy of Joel L. Cohen, MD. collagen loss and skin aging due to ESTROGEN What I found most impressive in the study by Dr. Draelos were the biopsies DEFICIENT SKIN, non-hormonally. showing the re-emergence of estrogen receptors on fibroblasts that had been dormant for years after menopause following application of MEP.

– Diane Berson, MD, FAAD

Blinded investigator-assessedMEP EXTENSIVELY % improvement STUDIED AND after CLINICALLY 14 weeks’ application PROVEN MEP* vs vehicle

 11%   P=0.001

*data on file Honing-in on Rejuvenation

Energy-based devices are known for their targeted approach Reducing Fluence Demand by over 50% to rejuvenation. Pinpointing targets or chromophores (including Because non-speci c skin heating is minimized using targeted pigment, melanin within hair follicles and skin, or hemoglobin wavelengths and dual-mode ltering, Ellipse IPL treats with for vascular treatments), these devices are typically designed less than half the fluence of broadband IPL.12 Excessive to maximize absorption ef cacy at the target and minimize any IPL uence is a major determinant of IPL risk, therefore potential negative impact of delivering excess minimizing fluence reduces risks such as energy to the target or nearby skin structures. scarring and hypo- and hyper pigmentation.7,9 Some energy-based system innovations go Additionally, using less uence has the advantage farther to focus energy and optimize safety of patient comfort12 as well as elimination of the design considerations. One such device is need for an external cooling device.7 the Nordlys™ multi-application platform, the The unique sub-millisecond pulse delivery only available multi-application system with capability on the Nordlys system provides narrowband intense pulsed light (IPL) and two further IPL improvement, allowing treatment of small 1-4,5 non-ablative laser resurfacing applicators. Together with a vascular lesions and diffuse redness.1,4,7 powerful Nd:YAG laser, these technologies create a exible, risk- minimizing platform with 21 FDA-cleared indications, including Innovations in Fractional, Non-Ablative Resurfacing benign pigmented and vascular lesions, and permanent hair Maximizing Wavelength Accuracy reduction in both lighter and darker skin types.1-4 The Nordlys system is the only multi-application platform Innovations in IPL with two fractional, non-ablative laser resurfacing The Nature of Intense Pulsed Light (IPL) technologies – addressing both shallow (Frax 1940™) 1-4 By nature, intense pulsed light is polychromatic, non- and deeper (Frax 1550™) resurfacing needs. With the coherent and unfocused.5 Early generation IPL systems, only 1940nm wavelength available in aesthetics, the Frax with wavelengths up to 1400nm6, increased risk to skin by 1940™ is the closest wavelength to the peak of water delivering unfocused broadband light, elevating skin thermal absorption at ~1935nm, delivering maximum accuracy to 13 impact.5 While effective and eventually mainstreamed, the the target compared to 1927nm thulium devices. devices were also known for their risk of burns, blisters, and Improving Treatment Reach hypo- or hyperpigmentation.11 Both Frax 1550™ (1550nm laser) and Frax 1940™ Narrowing Light Delivery applicators have adjustable treatment widths and pulse 7 Recent narrowband technology reigns in unfocused IPL. duration modi cation capability for customized treatment. In Narrowband IPL used in the Nordlys system (patented contrast to the leading competitive fractional device with xed Ellipse IPL™), focuses light wavelengths.7 The eight Ellipse treatment widths and a bulky thulium umbilical, the Frax diode IPL applicators have narrow wavelength range, creating laser applicators allow ease of treatment reach to the patient a more “laser-like” light band for targeting chromophores, and to more tricky treatment areas, notably around the nose 5,7 while reducing heat delivery and treatment risk.5,7 With water and eyes. lters in each handpiece and light ltered on both ends of Transforming Practice Costs the spectrum, the dual- ltering (water and light) technology For maximum practice savings, the replaceable roller on eliminates wavelengths above 950nm, a striking innovation the Frax 1550/Frax 1940 applicators allows high return- relative to earlier generation broadband light systems with on-investment (ROI) treatments at a low-cost of ~$26/ manually changeable light lters and more thermal delivery of treatment, significantly lower than earlier generation broadband light up to 1400nm.6,7 fractional non-ablative devices.5,7 Minimizing Number of Treatments Platform Innovations A clinical study of the treatment of telangiectasias with An integrated database helps guide treatment settings Ellipse IPL VL 555 (555-950 nm) and PR 530 (530-750nm) and retrievable patient history data simplifies treatment handpieces demonstrates that use of the more narrowband planning, while whisper quiet operation makes a calming PR applicator compared to the slightly broader band VL 555 experience for both practitioners and patients.5 applicator, reduces the number of treatment sessions needed.8

References 1. Ellipse Nordlys 510(k) clearance (K150907), July 2015. 2. Ellipse Frax 1550 510(k) clearance (K161162), Sept. 2016. 3. Ellipse Ydun Frax 1550 510(k) clearance (K180406), March 2018. 4. Ellipse Frax 1940 510(k) clearance (K192951), March 2020. 5. Data on File, Candela, 2021 6. Sciton BBL Hero speci cation, https://sciton.com/physicians/bbl/ 7. Nordlys User Manual, 2020. 8. Bjerring P, et al. Lasers Surg Med. 2004;34(2):120-126. 9. Thaysen‐Petersen, et al., Lasers Surg. Med., 49: 88-96. https:// doi.org/10.1002/lsm.22566 10. WebMD: https://www.webmd.com/beauty/intense-pulsed-light-treatment-overview#2 11. Philipp Babilas, MD, PhD,* et al., Lasers in Surgery and Medicine 42:93–104 (2010). 12. P Bjerring, et al., J Cosmetic & Laser Ther 2003; 5: 7–13#, J Cosmetic & Laser Ther. 13. Adapted from: D. M. Wieliczka and S. Weng and M. R. Querry, “Wedge shaped cell for highly absorbent liquids: infrared optical constants of water,” Appl. Opt., 28, 1714--1719, (1989). PU01814EN-NA, Rev. A Nordlys™ - Honing-in on Rejuvenation Ellipse IPL™ Pigmentation Vascularity

Nd:YAG 1064 Vascularity

Frax 1550™ and Frax 1940™ Skin Resurfacing Light changes everything. 1. Ellipse1. Frax Ydun clearance Pro 510(K) 1550, March (K180406), Ellipse 2018; Frax March clearance Pro 510(k) 1940, 2020; and Nordlys (K192951), 510(k) September Bjerringclearance 2. et 2016 al. Lasers Negishi 2. P, (K161162), Surg K, et al. Med. Dermatol 2004;34(2):120-126. Surg. 2006;32(11):1380-1387 © 2020 Candela Corporation. This material contains registered and unregisteredCorporation trademarks, and its affiliates. trade-names, All other trademarks service marksare the property and brand names of their of Candela respective owners. All rights reserved. Rev B. PU04151EN-NA

Not just any light. The right light. Nordlys’ Ellipse IPL technology with narrowband wavelengths, delivers targeted, controlled, filtered light - eliminating potentially harmful wavelengths above 950nm1. Compared to broadband wavelength devices, Ellipse IPL technology produces results in photodamaged skin with: • Half the fluence • No active cooling requirement • Fewer treatments2

The Nordlys system also includes the powerful light of Nd:YAG 1064 for vascularity, and non-ablative Frax 1550 and Frax 1940 for skin resurfacing without expensive consumables. Visit candelamedical.com/NordlysLight and discover how light changes everything.

Offer your patients the new skin illuminating treatment available exclusively on the Nordlys platform.

candelamedical.com | 800.733.8550

Untitled-1 1 6/2/21 1:52 PM It’s time for your treatment triumph

A CLINICALLY PROVEN PEPTIDE FORMULA THAT SUPPORTS ELASTIN AND COLLAGEN DEVELOPMENT

Regenerating Skin Nectar The Anti-Aging Powerhouse with TriHex Technology® is clinically proven ALASTIN Skincare’s TriHex Technology® Proves to Be the Best Companion to Procedures and a Daily Regimen Staple to help improve procedure recovery

• Prepares skin prior to a procedure and helps Laser resurfacing and other skin rejuvenation treatments are growing in popularity for good reason: These procedures can greatly improve “TriHex Technology is a peptide sequence that essentially to maximize procedure results the look and feel of skin and help patients reclaim a youthful glow. But systemizes the clearing of dysfunctional collagen and elastin when treatments are paired with procedure enhancement products from proteins in the ECM that have been broken down over time • Calms post-procedure skin and reduces the appearance of redness ALASTIN Skincare®, they become even more effective. ALASTIN’s products by the sun and various other factors, to make room for new • Helps reduce downtime and provides symptomatic relief are clinically proven to help downtime and outcomes—thereby boosting collagen and elastin,” explains DiAnne Davis, MD, a cosmet- patient satisfaction. ic dermatologist in Dallas. “Histologically, this process can • Patented TriHex Technology® helps to support the production show an improvement of collagen and elastin in as early as This journey starts two weeks before a procedure with the daily two weeks with compounded improvement over a year.” of new, healthy elastin and collagen application of ALASTIN’s Regenerating Skin Nectar with TriHex Technology® to prime the skin. It’s important to establish a healthy skin matrix to optimize procedure results. This is the “proof in the pudding” that aesthetic doctors have been waiting for, Dr. Davis says. “Not only do most of the products jumpstart the skin’s natural rejuvenation process by cleaning out the old collagen and elastin, but they also “ALASTIN has completed a multitude of studies to rebuild new healthy collagen and elastin that visibly results in a smoother tex- show how their formulations accelerate healing for ture, more hydrated skin, and enhanced elasticity and plumpness to the skin.” facial resurfacing, injectables, and body-sculpting procedures,” says Shino Bay Aguilera, DO, a Procedure Enhancement and Beyond Significant decrease in redness dermatologist and dermatologic surgeon in Fort Dr. Davis’ absolute favorite product is the Regenerating Skin Nectar. “I know and roughness on the Lauderdale, FL. “Implementing these products into it is going to add more bang for the buck when combining it with any of the your regular protocol takes a good experience to a procedures my patients are planning to do,” she says. “It also improves the Regenerating Skin Nectar side great experience for the patient, which is why this has recovery time with laser resurfacing procedures, and it has a nice silky feel become a regular part of my practice.” that glides onto the skin smoothly that all of my patients love.” 4 days post procedure For best results, Regenerating Skin Nectar should be used two weeks ahead The Power of TriHex Technology® of a procedure and two to four weeks afterward. Dr. Davis says that in order The benefits stem from ALASTIN Skincare’s patented TriHex Technology, to maximize the lasting benefits of a skin rejuvenation procedure, a patient specifically designed to clear out the inefficiencies of the extracellular matrix should keep TriHex Technology in their regimen. She suggests transitioning Untreated Treated with Regenerating Skin Nectar (ECM). TriHex Technology removes old, damaged collagen and elastin— to ALASTIN Skincare’s Restorative Skin Complex with TriHex Technology, while at the same time, supporting the skin’s natural ability to produce new a daily use product that helps restore volume, reduce pigmentation, and Footnote: Patient received the following regimen: (CeraVe® Cleansing Lotion, CeraVe® Cream, and Neutrogena®Ultrasheer® SPF 30). All subjects began using the basic skincare regimen to their collagen and elastin. protect the skin with antioxidants. entire face and the anhydrous gel with TriHex peptides (Regenerating Skin Nectar with TriHex Technology®, ALASTIN Skincare®, Carlsbad, CA) to the assigned side of the face twice daily until their next scheduled appointment, at least two weeks from the pretreatment visit. Procedure was hybrid fractional laser resurfacing using nonablative and ablative wavelengths of 1470 and 2940 nm, respectively (Halo™ Hybrid Fractional Laser; Sciton, Inc, Palo Alto, CA). “To continue the morning regimen, I recommend the Restorative Skin Reference: Nelson AM, Ortiz AE. Effects of anhydrous gel with TriHex peptides on healing after hybrid laser resurfacing. J Cosmet Dermatol. 2020;00:1–5. Complex to help balance the natural hydration that the skin needs, followed by one of my most absolute favorite sunscreens, the Hydratint Pro Mineral Broad-Spectrum Sunscreen SPF 36 that blends flawlessly with almost every skin tone,” Dr. Davis says. Ask your Skincare Professional about Regenerating Skin Nectar

A CLINICALLY PROVEN PEPTIDE FORMULA THAT SUPPORTS ELASTIN AND COLLAGEN DEVELOPMENT

Regenerating Skin Nectar with TriHex Technology® is clinically proven to help improve procedure recovery

• Prepares skin prior to a procedure and helps to maximize procedure results • Calms post-procedure skin and reduces the appearance of redness • Helps reduce downtime and provides symptomatic relief • Patented TriHex Technology® helps to support the production of new, healthy elastin and collagen

Significant decrease in redness and roughness on the Regenerating Skin Nectar side 4 days post procedure

Untreated Treated with Regenerating Skin Nectar

Footnote: Patient received the following regimen: (CeraVe® Cleansing Lotion, CeraVe® Cream, and Neutrogena®Ultrasheer® SPF 30). All subjects began using the basic skincare regimen to their entire face and the anhydrous gel with TriHex peptides (Regenerating Skin Nectar with TriHex Technology®, ALASTIN Skincare®, Carlsbad, CA) to the assigned side of the face twice daily until their next scheduled appointment, at least two weeks from the pretreatment visit. Procedure was hybrid fractional laser resurfacing using nonablative and ablative wavelengths of 1470 and 2940 nm, respectively (Halo™ Hybrid Fractional Laser; Sciton, Inc, Palo Alto, CA). Reference: Nelson AM, Ortiz AE. Effects of anhydrous gel with TriHex peptides on healing after hybrid laser resurfacing. J Cosmet Dermatol. 2020;00:1–5.

Ask your Skincare Professional about Regenerating Skin Nectar

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A s n G i u x id to in aesthetics e ro t u Topics• BREAST IMPLANT SAFETY o t Ne he ng • HAIR TRANSPLANTATION SURGERY Expandi • CONTROL YOUR PRACTICE DESTINY • NO TOUCH PRACTICE • DIVERSITY IN AESTHETICS EXPERT TIPS FOR BUILDING YOUR BRAND LOW INTEREST RATES AND UP YOUR SOCIAL MEDIA COVID-19 UPDATES INVESTING: MAKING SENSE COVID-19 UPDATES INVESTMENT OPPORTUNITIES MARKETING GAME MODERNAESTHETICS.COM/COVID-19 TIME TO RETHINK MATV: EXPRESSIVE FACING THE GENERATION BOARD FORUM: OF THE MARKETS TAKE 5 WITH SOLITON; REVANCE MODERNAESTHETICS.COM/COVID-19 FILLERS GAP IN MARKETING BUILDING A BRAND VIRTUAL CONSULTS?

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EXPLORE A SPECTRUM OF OPPORTUNITIES FOR SUCCESS, FROM VIRTUAL EVENTS TO SPA OVERSIGHT AND MORE Navigate a course for your practice ONLINE REVIEWS: THREE WAYS: DO NOW TIPS COVID-19 UPDATES WHAT TO KNOW ABOUT OMNICHANNEL MARKETING DISCOUNTING DONE RIGHT: TIPS FOR SUCCESS HOW TO BE PROACTIVE FOR FUTURE SUCCESS MODERNAESTHETICS.COM/COVID-19 AVOID BURNOUT CORRECTING CONTRACTS EHR PITFALLS PROTECT YOUR MEDSPA

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SEPTEMBER/OCTOBER 2016 | VOL. 4, NO. 5 MODERNAESTHETICS.COM MARCH/APRIL 2019 | VOL. 7, NO. 2 MODERNAESTHETICS.COM JULY/AUGUST 2021 | VOL.9, NO. 4 | MODERNAESTHETICS.COM

SOCIALSOCIAL CUESCUES Spotting trends for success with social media in aesthetic medicine.

Opportunities—and challenges— face aesthetic physicians as they mold their future • The Cost of Poor Leadership • What’s Valuable in a Practice? • Understanding Employment Options Hot • New Practice Models • The Perils of Commoditization

How to sell expertise, not services ACKNOWLEDGEMENT: KEY TO HOW MASKING MAY AFFECT ESTATE PLANNING: WHAT SCAN FOR COVID-19 BETTER PATIENT ENCOUNTERS POST-PROCEDURE HEALING YOU NEED TO CONSIDER UPDATES SHOULD YOU CONSIDER MUNI s? GIVING MEANINGFUL FEEDBACK HOW TO RECOVER FROM BAD ADVICE MA/TV: AAFPRS CommodityCONTOUR CULTURE: ALL IN THE FAMILY: IT’S A SNAP: SOCIAL MEETING UPDATES REVOLUMIZATION PEARLS WORKING WITH LOVED ONES MEDIA’S LATEST CRAZE

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PREPARING FOR WHAT’S NEXT Where to invest now for future success

STATE of THE

Aesthetics Crosses Gender Lines MATV: A GLOBAL MILESTONE MARKETING: BOARD FORUM: STATUS THREE WAYS: HOW MA/TV: THE MALE SEO: IMPLICATIONS OF STOP NEGLECTING IT: FINANCIAL PLANNING: NEW PERSPECTIVE ON MILLENNIALS COPING WITH COVID-19 SERIES & UPDATES: MODERNAESTHETICS.COM VIEW ON INJECTABLES PATIENTS FOR LIFE OF AESTHETIC MEDICINE TO SPEND $10K TOXIN TREND MACHINE LEARNING COMPETITIVE ADVANTAGE MORE COMMON TRAPS

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JULY/AUGUST 2015 | VOL. 3, NO. 4 MODERNAESTHETICS.COM

YOUR TRUSTED SOURCE FOR EVERYTHING AESTHETICS

MA/TV: EXPERT INSIGHTS BOARD FORUM: WHAT’S NEXT: THE EXPANDING DEADLY SINS OF FROM DEVICE TALK SUCCESSFUL DEVICE ACQUISITION ROLE OF SKIN CARE MEDICAL MARKETING

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JANUARY/FEBRUARY 2016 | VOL. 4, NO. 1 MODERNAESTHETICS.COM JANUARY/FEBRUARY 2015 | VOL. 3, NO. 1 MODERNAESTHETICS.COM NOVEMBER/DECEMBER 2017 | VOL. 5, NO. 6 MODERNAESTHETICS.COM

LETTING GO TO RECLAIM YOUR SANITY. Blinded by the Plight Don’t let fear of noncompliance make you overlook important opportunities.

MATV: AAFPRS UPDATES, MILLENNIAL WORKFORCE: THINK BEFORE YOU TEXT: LIVE SURGERY: MA/TV: OPTIMAL BOARD FORUM: BRIDGING NEW COSMECEUTICALS: MARKETING: YOU NEED MA/TV: QUITTING A GROUP EMRS: ASSESSING BENEFITS, RISKS, AND THE SAYING GOODBYE TO COMING & GOING: IS MICRONEEDLING FILLERS OVERVIEW OPTIMIZE RELATIONSHIPS HIPAA & TECHNOLOGY MAKE IT WORK APPROACHES TO LIPS THE GENERATION GAPS ASSESSING TOPICAL PROBIOTICS LONG-RANGE PLANS TO START A SOLO PRACTICE DECISION TO GIVE UP INCENTIVES THE CHALLENING PATIENT REALLY THE NEXT BIG THING?

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