Ұ Based on warranty comparisons of the following breast implants. The third‐party trademarks used herein are the trademarks of the respective owners.

*In‐person consumer survey with 452 respondents.

1. Mentor Worldwide LLC. Mentor Worldwide Historical Implant Data Jun 2018‐ Jan 2020. January 2020.

2. Based on warranty comparisons of the following breast implants. Motiva^® Warranty Program Terms and Conditions. Motiva, 2018. A Continued Commitment to Patients BIOCELL^® Replacement Warranty. Allergan, 2019. Polytech. IMPLANTS OF EXCELLENCE PROGRAMME. Professional Service for Patients with POLYTECH Implants, 2019. GCA Comfort Guarantee. Nagor and Eurosilicone breast implants. Website: shorturl.at/aoGIR. Access date: 5/13/2020.

3. MENTOR Consumer Preference Market Research Report ‐ July 2017

4. SALINE-FILLED SPECTRUM^TM BREAST IMPLANTS. PPE Specification Labeling Specification 102926-001 Rev D Saline-Filled Spectrum Breast Implants CE-Marked PIDS. 2016. Page.15.

5. David Overaker Stephan Rothenbuguer. 3D Imaging of comfort, CPX2/3, and Allergan style 133 Tissue Expanders for Shape and Strain Measurement, AST‐ 2012‐0176. Page 2, 11 (par.2). 5.2.102983‐001 Rev D MENTOR CPX4 CPX4 WITH SUTURE TABS BREAST TISSUE EXPANDERS CE‐MARKED PIDS 100149058 | Rev:4 Released: 19 Dec 2017. Page 1, 7 (par. 1, 2, 5).

6. Hammond DC, Canady JW, Love TR, et al. Mentor Contour Profile Gel Implants: Clinical Outcomes at 10 Years Plastic Reconstr Surg, 2017.

Important Safety Information:

The MENTOR^® Collection of Breast Implants are indicated for breast reconstruction and breast augmentation - in women who are at least 18 years old for MENTOR^® MemoryGel^® Breast Implants, MENTOR^® CPG^TM Breast Implants, or MENTOR^® Saline Breast Implants.

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. The chance of developing complications increases over time. 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^® Implants include any reoperation, capsular contracture, nipple sensation changes, and implant removal with or without replacement. The most common complications with CPG^TM Breast Implants for breast augmentation include reoperation for any reason, implant removal with or without replacement, and ptosis. 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. Breast implants are also associated with the risk of breast implant-associated anaplastic large cell lymphoma (BIA-ALCL), an uncommon type of lymphoma. An individual's risk of developing BIA-ALCL with MENTOR^® Breast Implants is low based on the data currently available on the incidence of worldwide cases.

Detailed information regarding the risks and benefits associated with MENTOR^® Breast Implants is provided in several educational brochures, including the ‘Important Information for Woman Considering Breast Implants’ brochure, and the ‘Making an Informed Decision’ brochure. These brochures are available from your surgeon or visit https://breastimplantsbymentor.net/safety/mentor-safety. It is important that you read and understand these brochures when considering MENTOR^® Breast Implants.

MENTOR^® CONTOUR PROFILE^TM Breast Tissue Expanders are used for breast reconstruction after mastectomy, correction of an underdeveloped breast, scar revision, and tissue defect procedures. These expanders are intended for temporary subcutaneous or submuscular implantation; they should be used within a time frame determined by the physician to achieve the clinically desired degree of tissue expansion.

DO NOT use the MENTOR^® CONTOUR PROFILE^TM Tissue Expander in patients that have a previously implanted device such as pacemakers, drug infusion devices, artificial sensing devices, etc. that could be affected by a magnetic field. Mentor has not tested the effects of radiation therapy with the MENTOR^® CONTOUR PROFILE^TM Expander devices. The incidence of extrusion of the expander has been shown to increase when the expander has been placed in injured areas: scarred, heavily irradiated or burned tissue, crushed bone areas, where severe surgical reduction of the area has previously been performed; and where steroids are used in the surgical pocket. Detailed information about indications, contraindications, warnings, and precautions associated with the use of MENTOR^® CONTOUR PROFILE^TM Expanders are provided in the Instructions for Use (IFU) available online at www.mentorwwllc.eu

The third-party trademarks used herein are the trademarks of the respective owners.
This publication is not intended for distribution outside of the EMEA region.