Intended for healthcare professionals

MENTOR™ ARTOURA™ PLUS Breast Tissue Expanders

The MENTOR™ ARTOURA™ PLUS Breast Tissue Expander is designed to withstand hugs, naps, and all her everyday pressures with proprietary pocket precision.1,2 


The MENTOR™ ARTOURA™ PLUS Breast Tissue Expander is the only expander with Dynamic Control Technology™, delivering a precise1,2 and predictable pocket.2A

About this device

The MENTOR™ ARTOURA™ PLUS Breast Tissue Expander maximizes lower pole projection while minimizing superior pole distortion, and minimizing lateral, medial, and posterior wall protrusion. It is the only expander with Dynamic Control Technology™ for unsurpassed control and predictability.2,3A

Specialties

Breast Reconstruction

Procedures

Breast Reconstruction

Pocket precision1,2

  • Limited Superior Pole Distortion
  • Limited Posterior Distortion
  • Maximum Lower Pole Projection

Technology

  • BufferZone™ Self-Sealing Patch to protect at least 50% more surface area from accidental needle puncture and deflation, the leading cause of device failure.
  • Battery-free CENTERSCOPE™ Magnetic Detection Device effortlessly locates the magnetic injection dome for ease and accuracy4
  • Dynamic Control Technology™ regulates upper pole, lower pole, and lateral expansion limits posterior distortion2

Supporting documentation

PDF

MENTOR Product Catalog

PDF

MENTOR Company Overview One-Pager

PDF

MemoryGel Implants and Tissue Expanders Order Form
Select all (3)

Related products

References

Warning
  • Breast implants are not considered lifetime devices. The longer people have them, the greater the chances are that they will develop complications, some of which will require more surgery.
  • Breast implants have been associated with the development of a cancer of the immune system called breast implant-associated anaplastic large cell lymphoma (BIA-ALCL). This cancer occurs more commonly in patients with textured breast implants than smooth implants, although rates are not well defined. Some patients have died from BIA-ALCL.
  • Patients receiving breast implants have reported a variety of systemic symptoms such as joint pain, muscle aches, confusion, chronic fatigue, autoimmune diseases and others. Individual patient risk for developing these symptoms has not been well established. Some patients report complete resolution of symptoms when the implants are removed without replacement.

A. As compared to Allergan 133MV-13 and 133MX-13 in a benchtop study under simulated compression

  1. FM-0001306_v6 Flexa Design Requirements Matrix
  2. 100316549 3D Benchtop Imaging of Artoura and Allergan Completion Report
  3. Vertical Compression Report 100890446, Testing of ARTOURA PLUS Smooth Breast Tissue Expanders.
  4. The Instructions for Use for the MENTOR™ CPX™4 and CPX™4 with Suture Tabs Breast Tissue Expanders, LAB100835493v2, 2022


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


The sale and distribution of Mentor Breast Implant Devices are restricted to users and/or user facilities that provide information to patients about the risks and benefits of the device prior to its use in the form and manner specified in approved labeling to be provided by Mentor Worldwide LLC.


Important information: Prior to use, refer to the instructions for use supplied with this device for indications, contraindications, side effects, warnings and precautions.


Caution: US law restricts this device to sale by or on the order of a physician.


Important Safety Information

The ARTOURA™ Breast Tissue Expander and CONTOUR PROFILE™ Breast Tissue Expander are used 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. Do not use the ARTOURA™ Tissue Expander nor CONTOUR PROFILE™ Tissue Expander in patients where an MRI may be needed. The device could be moved by the MRI causing pain or displacement, potentially resulting in a revision surgery. 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 mentorwwllc.com.


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


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