RHIS 2020 Exhibitor Flipbook

RHIS 2020 Annual Scientific Meeting

Exhibitor Flipbook

SKINPEN PRECISION ®

THE HIGHEST STANDARD “ I can’t see any reason for a physician-directed practice not to own a SkinPen device.”

— Jenni Holman, Dermatologist, U.S. Dermatology Partners

 1st FDA-Cleared Microneedling Device  90% of clinical trial subjects were happy with their results and would recommend to friends and family1  96% of our customers expressed high satisfaction2

Discover the Superiority of SkinPen PREMIER DESIGN The ONLY U.S.A. engineered and manufactured microneedling pen with the versatility of a cordless device and continuous power through inductive charging

SAFE AND EFFECTIVE Excelled in 90+ validation tests and is proven safe for ALL Skin Types (Fitzpatrick 1 – 6)

HIGH PROFITABILITY Quick and easy procedure and most SkinPen treatments have an ROI of over 500%

3 new patients/week 3 treatments/patient $350/treatment $163,800 annual revenue *

LEARN MORE TODAY AT SKINPEN.COM

SkinPen Precision is the first FDA-cleared Microneedling device. 1SkinPen U.S. intended use: The SkinPen Precision System is a microneedling device and accessories intended to be used as a treatment to improve the appearance of facial acne scars in adults aged 22 years and older. Rx only. 2Bellus Customer Satisfaction Survey March 2019 (data on file). *US national avg. cost ©2020 Crown Aesthetics. | PN# LIT200908.01

Comprehensive Solutions for Deformity Correction RAPIDSORB® Injectable Polymer System Cordless Resorbable Fixation for Cranial Vault Reconstruction ■ Multiple fastener length options allow an optional bolus of polymer on the bone’s underside ■ Significantly decreases surgeon workload vs SonicWeld Rx1 ■ Surgeons preferred IPS over SonicWeld Rx1

TRUMATCH® CMF Personalized Solutions Fully personalized solutions to help achieve accuracy, efficiency, and patient benefit, for even the most complex surgeries

Virtual surgical planning and guides for cranial vault reconstruction

Titanium 3D printed guides and plates for facial reconstruction and orthognathic surgery

Family of Distractors ■ Curvilinear Distraction System allows surgeons to correct complex mandible deformities with an internal distractor and is compatible with TRUMATCH® CMF Personalized Solutions planning and guides ■ External Midface Distractor provides user-friendly, versatile, and secure distraction of the midface and cranium Related Products ViviGen® and ViviGen Formable® Cellular Bone Matrix Osteogenic, osteoconductive, and osteoinductive allograft bone void filler 2

Tissue And Palatal Retractor Set A dedicated instrument set for cleft lip and palate repair with unique retractors

Piezoelectric System Ultrasonic surgical system cuts mineralized bone; soft tissue sparing

We offer comprehensive solutions for deformity correction.

ViviGen® and ViviGen Formable® are registered trademarks of LifeNet Health.

1. Cranial Fixation System Time and Motion Comparison Study. Design Sciences.

November 2016.

Manufactured or distributed by: Synthes USA Products, LLC 1302 Wrights Lane East West Chester, PA 19380

2. Data on file at LifeNet Health DHF 12-008.

Synthes USA, LLC 1101 Synthes Avenue Monument, CO 80132

To order (USA): 800-523-0322 Note: For recognized manufacturer, refer to the product label. www.depuysynthes.com

Limited Warranty and Disclaimer: DePuy Synthes products are sold with a limited warranty to the original purchaser against defects in workmanship and materials. Any other express or implied warranties, including warranties of merchantability or fitness, are hereby disclaimed.

Please also refer to the package insert(s) or other labeling associated with the devices identified in this sell sheet for additional information.

CAUTION: Federal Law restricts these devices to sale by or on the order of a physician.

Some devices listed in this sell sheet may not have been licensed in accordance with Canadian law and may not be for sale in Canada. Please contact your sales consultant for items approved for sale in Canada.

Not all products may currently be available in all markets.

© DePuy Synthes 2019. All rights reserved.

110562-190328 DSUS 05/19 DV

The third party trademarks used herein are the trademarks of their respective owners.

Have You Felt the

MENTOR® MemoryGel® Xtra Breast Implant?

In a blinded comparison 9 out of 10 consumers chose MemoryGel® Xtra Breast Implants as feeling more like a natural breast than the other leading brand.*1

@BreastImplantsbyMentor #MemoryGelXtra #MentorBreastImplants #OwnTheDay *Head-to-head blinded in-person tabletop product comparison (MemoryGel Xtra vs. Inspira Responsive vs. Inspira Cohesive) with 452 respondents. 1. Mentor Consumer Preference Market Research Report - July 2017.

IMPORTANT SAFETY INFORMATION MENTOR® MemoryGel® Breast Implants are indicated for breast augmentation in women who are at least 22 years old. Breast implant surgery should not be performed in women: With active infection anywhere in their body; With existing cancer or pre-cancer of their breast who have not received adequate treatment for those conditions; Who are currently pregnant or nursing. Safety and effectiveness have not been established in patients with autoimmune diseases (for example lupus and scleroderma), a weakened immune system, conditions that interfere with wound healing and blood clotting, or reduced blood supply to breast tissue. Patients with a diagnosis of depression, or other mental health disorders, should wait until resolution or stabilization of these conditions prior to undergoing breast implantation surgery.

There are risks associated with breast implant surgery. You should be aware that breast implants are not lifetime devices and breast implantation may not be a one-time surgery. You may need additional unplanned surgeries on your breasts because of complications or unacceptable cosmetic outcomes. Many of the changes to your breast following implantation are irreversible (cannot be undone) and breast implants may affect your ability to breastfeed, either by reducing or eliminating milk production.

Breast implants are not lifetime devices and breast implantation may not be a one-time surgery. The most common complications for breast augmentation with MemoryGel® Breast Implants include any reoperation, capsular contracture, nipple sensation changes, and implant removal with or without replacement. A lower risk of complication is rupture. The health consequences of a ruptured silicone gel breast implant have not been fully established. MRI screenings are recommended three years after initial implant surgery and then every two years after to detect silent rupture.

Detailed information regarding the risks and benefits associated with MENTOR® Breast Implants is provided in the educational brochure for MemoryGel® Implants: Important Information for Augmentation Patients about MENTOR® MemoryGel® Breast Implants. The brochure is available from your surgeon or visit www.mentorwwllc.com. It is important that you read and understand the brochure when considering MENTOR® MemoryGel® Breast Implants. © Mentor Worldwide LLC 2019 109944-190320

Convenience for you, radiance for your patients.

Off-the-shelf allograft alternative to small volume fat grafting

Pre-cut coastal cartilage allograft for rhinoplasty patients

mtfbiologics.org/RHIS

A more efficient fat-grafting solution

her breast reconstruction journey begins here A portfolio of options for you, a more personalized approach for her.

®

BREAST RECONSTRUCTION

A comprehensive portfolio of breast tissue expanders and silicone gel breast implants uniquely designed to reduce risk and improve patient outcomes.1,2

To learn more about Sientra OPUS Breast Reconstruction products please call 1.888.708.0808 For more information, go to www.discover.sientra.com/SientraBreastReconstruction 1. Stevens WG, Calobrace MB, Alizadeh A, Zeidler KR, Harrington JL, d’Incelli RC. Ten-year core study data for Sientra’s Food and Drug Administration - approved round and shaped breast implants with cohesive silicone gel. Plast Reconstr Surg. 2018;141(4S):7S-19S 2. Fairchild B, Ellsworth W, Selber JC, Bogue DP, Zavlin D, Nemir S, Checka CM, Clemens MW. Safety and Efficacy of Smooth Surface Tissue Expander Breast Reconstruction. Aesth Surg. Volume 40, Issue 1, January 2020, Pages 53–62, https://doi.org/10.1093/asj/ sjy199 Sientra breast tissue expanders are indicated for breast reconstruction. They are temporary expanders and are not intended for long-term or permanent implantation. Sientra breast tissue expanders are contraindicated in patients with active infection or existing carcinoma at the intended expansion site. Tissue Expanders with integral magnetic ports should not be used in patients who already have implanted devices subject to magnetic field interference or in patients where an MRI may be needed. Prior to use, plastic surgeons should review the Instructions for Use and detailed information regarding the risks and benefits of Sientra breast tissue expanders, located at sientra.com.

Sientra OPUS breast implants are indicated for breast augmentation in women at least 22 years old and for breast reconstruction. Breast implant surgery is contraindicated in women with active infection anywhere in their body; with existing cancer or precancerous conditions who have not received adequate treatment for those conditions and; who are currently pregnant or nursing. Prior to use, plastic surgeons should review all risk information, which is found in the Instructions for Use. Key complications associated with the use of silicone gel breast implants include capsular contracture, implant removal, rupture and reoperation. The Instructions for Use and detailed information regarding the risks and benefits of Sientra OPUS breast implants can be found at sientra.com/resources.

Sientra® and OPUS® are trademarks of Sientra, Inc. © 2020 Sientra, Inc. All rights reserved. U.S. Patent: #8,454,690 MDC-0459 R1

NOBODY LIKES DOING IT OVER. What if there was a better way?

A successful hernia repair sometimes requires more than just skill, and providing surgeons with innovative technology can be a challenge in today’s constrained healthcare environment.

That’s why TELA Bio purposefully designed advanced soft tissue reinforcement solutions that can increase positive patient outcomes while helping hospitals reduce their hernia mesh costs.

Download our eBook to discover how we’re working to improve hernia surgery for your surgeons, your patients, and your bottom line.

Download at TELABIO.com/purposefuldesign

1 (844) 835-2246