MENTOR® Volume Sizing System

Introducing the MENTOR® Volume Sizing System. Eighteen volume sizing devices designed to help your patient feel invested in her size decision and satisfied with her result. Featuring a unique shape that fits over her natural breast, creating a more realistic preview of her new size. All provided in a high-quality clear, acrylic display case for ease of storage and presentation.

volume sizing system

Features & Benefits

volume sizing

Patient Impact

82% of surgeons surveyed stated the Sizing System had a high impact on patient conversions. Surveyed surgeons indicated the Sizing System could lower augmentation reoperation rates due to size change.1 These tools are meant to assist you in selecting the right implant to achieve the patient’s desired results. The MENTOR® Volume Sizing System does not dictate a specific implant, but provides guidance in selecting a range of devices that will increase the likelihood of patient satisfaction. 

The MENTOR® Volume Sizing System is not intended to replace your independent professional judgment. 

Product Resources

Ordering Replacement Sizers

Over time you may need to reorder additional individual sizers. See below for catalog numbers specific to each sizer.

Product Name

Catalog Number

MENTOR® Volume Sizing Device – 50 cc


MENTOR® Volume Sizing Device – 75 cc


MENTOR® Volume Sizing Device – 125 cc


MENTOR® Volume Sizing Device – 150 cc


MENTOR® Volume Sizing Device – 250 cc


MENTOR® Volume Sizing Device – 350 cc


MENTOR® Volume Sizing Device – 450 cc


MENTOR® Volume Sizing Device – 550 cc


MENTOR® Volume Sizing Device – 650 cc



Carton contains four sterile kits. Each kit contains the following:


Catalog #

MENTOR® Volume Sizing System - Display Case + Volume Sizers



*A customer is able to purchase replacement units only following the purchase of the
MENTOR® Volume Sizing System (ESZKIT).

PLEASE NOTE: Individual implant dimensions may vary slightly in products of this type.
Not all units conform exactly to the dimensions noted above.

Product Catalog

Product Catalog

Important Information for Your Patients to Consider

Important Information for Women Considering Breast Implants


1. LEAD Survey Questionnaire – May 2011

Important Safety Information

MENTOR® MemoryGel® Breast Implants, MENTOR® MemoryShape® Breast Implants, and MENTOR® Saline-filled Breast Implants are indicated for breast augmentation in women (at least 22 years old for MemoryGel® Implants and MemoryShape® Implants, and 18 years old for Saline Implants) or for breast reconstruction. 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, or who are currently pregnant or nursing.

Breast implants are not lifetime devices and breast implantation may not be a one-time surgery. The chance of developing complications increases over time. The most common complications for breast augmentation and reconstruction with MemoryGel® Implants include any reoperation, capsular contracture, and implant removal with or without replacement. The most common complications with MemoryShape® Implants for breast augmentation include reoperation for any reason, implant removal with or without replacement, and ptosis. The most common complications with MemoryShape® Implants for breast reconstruction include reoperation for any reason, implant removal with or without replacement, and capsular contracture. 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 incidence of worldwide cases. The most common complications with MENTOR® Saline-filled Implants include reoperation, implant removal, capsular contracture, breast pain, and implant deflation.

For MemoryGel® Implants, patients should receive a copy of Important Information for Augmentation Patients about MENTOR® MemoryGel® Breast Implants or Important Information for Reconstruction Patients about MENTOR® MemoryGel® Breast Implants. For MemoryShape® Implants, patients should receive a copy of Patient Educational Brochure – Breast Augmentation with MENTOR® MemoryShape® Breast Implants or Patient Educational Brochure – Breast Reconstruction with MENTOR® MemoryShape® Breast Implants, and a copy of Quick Facts about Breast Augmentation & Reconstruction with MENTOR® MemoryShape® Breast Implants. For MENTOR® Saline-filled Implants, patients should receive a copy of Saline-Filled Breast Implants: Making an Informed Decision. Your patient needs to read and understand the information regarding the risks and benefits of breast implants, with an opportunity to consult with you prior to deciding on surgery.

The ARTOURA® Breast Tissue Expander or CONTOUR PROFILE® Breast Tissue Expander can be utilized for breast reconstruction after mastectomy, correction of an underdeveloped breast, scar revision, and tissue defect procedures. The expander is intended for temporary subcutaneous or submuscular implantation and is not intended for use beyond six months. ARTOURA® Breast Tissue Expander and CONTOUR PROFILE® Tissue Expanders include magnetic injection domes, which contain a rare earth permanent magnet, and are NOT MRI compatible. The device could be moved by the MRI causing pain or displacement, potentially resulting in a revision surgery. Do not use the ARTOURA® Tissue Expander nor CONTOUR PROFILE® Tissue Expander in patients where an MRI may be needed. DO NOT use the ARTOURA® Breast Tissue Expander and CONTOUR PROFILE® 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 in vivo effects of radiation therapy with ARTOURA® Breast Tissue Expander and CONTOUR PROFILE® Expander devices and cannot warrant the safety of such use. 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.

For detailed indications, contraindications, warnings, and precautions associated with the use of all MENTOR® Implantable Devices, which include MENTOR® Saline-filled Implants, MemoryGel® Implants, MemoryShape® Implants, ARTOURA® Expanders, and CONTOUR PROFILE® Expanders, please refer to the Instructions for Use (IFU) provided with each product or visit