Tits Simulator

Tits Simulator
Adjust size of brush to be slightly bigger than areola.
Click first breast and drag away from center of brush until desired breast size is achieved.
Use Un-reshape tool to correct unwanted distortion. To use Un-reshape tool, simply click and drag distorted area. Running the tool down the side of the arms will correct distortion of the arms.
Correct areola size by moving brush over areola and clicking one or two times as desired.
If wanted, lift breasts. Select Reshape tool, resize brush so that brush is just smaller than the breast size, and lift breasts slightly by clicking and dragging each breast upwards.
Click before/after menu item to compare the simulated result to the original, side by side!
Breast augmentation is surgery to increase breast size or correct asymmetry. Implants are surgically placed underneath the breast tissue or chest muscles. If you're thinking
about getting breast augmentation surgery, FaceTouchUp’s Virtual Plastic Surgery Simulator
can help you experiment and visualize different surgical outcomes.

Uploading your own photos is quick and easy, both side profile and frontal body photos are supported. Try as many different outcomes as you like, while you enjoy the privacy
of your own home. Once you're done, you can send or print your before and after photos to give to your plastic surgeon for review.

In addition to breast augmentation simulation, FaceTouchUp
can also be used for breast lift procedures as well! Learn more here.
FaceTouchUp is the #1 app used by patients and surgeons alike, to visualize elective ‘before & after’ surgery results. Our plastic surgery simulation technology is
available in web, mobile, desktop, and SDK editions. FaceTouchUp can be used independently by patients or through partnering clinics that offer branded versions on their
websites and mobile apps.

We are based in beautiful Raleigh, North Carolina. To contact us, please email info@facetouchup.com
or call us toll-free at 1-888-828-1423.

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Home / News / Bouncing breast simulator
2022 Concept&Design: MOJOBRANDS | Copyright © BULA Ltd
Shock Absorber, a UK line of sports-bras, has a Flash-based boobies-physics simulator. Plug in a cup-size and a level of activity, and it produces a 3D animation of breasts of that size bouncing free, bouncing in a regular bra, and hardly moving at all in one of their sports-bras. Extra geeky bonus points for including a 3D wireframe view, so you can see the pure physics of the jiggle. Link
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Use our Visualizer tool to create a custom breast implant profile for a physician consultation.
MENTOR ® Visualizer powered by ILLUSIO See it in action
The third party trademarks used herein are the properties of their respective owners
Important Safety Information and Boxed Warning for MENTOR ® Breast Implants

Important Safety Information and Boxed Warning for MENTOR ® Breast Implants
© Mentor Worldwide LLC 2021 115302-211018 All Rights Reserved.
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 systematic 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.
Caution: US law restricts this device to sale by or on the order of a physician.

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.

The MENTOR ® Collection of Breast Implants are indicated for breast augmentation - in women who are at least 22 years old for MENTOR ® MemoryGel ® Breast Implants or MENTOR ® MemoryShape ® Breast Implants, and at least 18 years old for MENTOR ® Saline Breast Implants. MENTOR ® Breast Implants are also indicated for breast reconstruction.
Breast implant surgery should not be performed in women:
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.
Consult your physician for a full discussion of risks and benefits to determine whether this procedure is right for you. The success of this procedure depends on many factors, including your physical condition and your body’s ability to tolerate the procedure. Use care in the selection of your doctors and hospital, based on their skill and experience.
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 MemoryShape ® Implants for breast augmentation include reoperation for any reason, implant removal with or without replacement, and ptosis. The most common complications for breast reconstruction with MENTOR® MemoryGel® Breast Implants include any reoperation, implant removal with or without replacement, and capsular contracture. The most common complications with MENTOR® MemoryShape® Breast Implants for breast reconstruction include reoperation for any reason, implant removal with or without replacement, and capsular contracture. The most common complications for breast reconstruction with MENTOR® Saline-filled Breast Implants include re-operation, implant removal, capsular contracture, breast pain, and implant deflation. 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.
Detailed information regarding the risks and benefits associated with MENTOR ® Breast Implants is provided in several educational brochures for both augmentation and reconstruction:
For Augmentation: Important Information for Augmentation Patients about MENTOR ® MemoryGel® Breast Implants. Patient Educational Brochure – Breast Augmentation with MENTOR ® MemoryShape ® Breast Implants and Quick Facts about Breast Augmentation & Reconstruction with MENTOR ® MemoryShape ® Breast Implants.
For Reconstruction: Important Information for Reconstruction Patients about MENTOR ® MemoryGel ® Breast Implants. Patient Educational Brochure – Breast Reconstruction with MENTOR ® MemoryShape ® Breast Implants and Quick Facts about Breast Augmentation & Reconstruction with MENTOR ® MemoryShape ® Breast Implants.
Saline-Filled Breast Implants: Making an Informed Decision.
These brochures are available from your surgeon or visit www.mentorwwllc.com . It is important that you read and understand these brochures when considering MENTOR® Breast Implants.
ARTOURA ® Breast Tissue Expanders and CONTOUR PROFILE ® Breast Tissue Expanders 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 Expanders and CONTOUR PROFILE ® Tissue Expanders contain a magnet within the internal injection domes 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 ® 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 effects of radiation therapy with ARTOURA ® Breast Tissue Expanders and CONTOUR PROFILE ® 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 ARTOURA® Breast Tissue Expanders and CONTOUR PROFILE ® Expanders are provided in the Instructions for Use (IFU) available online at www.mentorwwllc.com
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 systematic 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.
Caution: US law restricts this device to sale by or on the order of a physician.

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.

The MENTOR ® Collection of Breast Implants are indicated for breast augmentation - in women who are at least 22 years old for MENTOR ® MemoryGel ® Breast Implants or MENTOR ® MemoryShape ® Breast Implants, and at least 18 years old for MENTOR ® Saline Breast Implants. MENTOR ® Breast Implants are also indicated for breast reconstruction.
Breast implant surgery should not be performed in women:
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.
Consult your physician for a full discussion of risks and benefits to determine whether this procedure is right for you. The success of this procedure depends on many factors, including your physical condition and your body’s ability to tolerate the procedure. Use care in the selection of your doctors and hospital, based on their skill and experience.
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 MemoryShape ® Implants for breast augmentation include reoperation for any reason, implant removal with or without replacement, and ptosis. The most common complications for breast reconstruction with MENTOR® MemoryGel® Breast Implants include any reoperation, implant removal with or without replacement, and capsular contracture. The most common complications with MENTOR® MemoryShape® Breast Implants for breast reconstruction include reoperation for any reason, implant removal with or without replacement, and capsular contracture. The most common complications for breast reconstruction with MENTOR® Saline-filled Breast Implants include re-operation, implant removal, capsular contracture, breast pain, and implant deflation. 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.
Detailed information regarding the risks and benefits associated with MENTOR ® Breast Implants is provided in several educational brochures for both augmentation and reconstruction:
For Augmentation: Important Information for Augmentation Patients about MENTOR ® MemoryGel® Breast Implants. Patient Educational Brochure – Breast Augmentation with MENTOR ® MemoryShape ® Breast Implants and Quick Facts about Breast Augmentation & Reconstruction with MENTOR ® MemoryShape ® Breast Implants.
For Reconstruction: Important Information for Reconstruction Patients about MENTOR ® MemoryGel ® Breast Implants. Patient Educational Brochure – Breast Reconstruction with MENTOR ® MemoryShape ® Breast Implants and Quick Facts about Breast Augmentation & Reconstruction with MENTOR ® MemoryShape ® Breast Implants.
Saline-Filled Breast Implants: Making an Informed Decision.
These brochures are available from your surgeon or visit www.mentorwwllc.com . It is important that you read and understand these brochures when considering MENTOR® Breast Implants.
ARTOURA ® Breast Tissue Expanders and CONTOUR PROFILE ® Breast Tissue Expanders 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 Expanders and CONTOUR PROFILE ® Tissue Expanders contain a magnet within the internal injection domes 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 ® 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 effects of radiation therapy with ARTOURA ® Breast Tissue Expanders and CONTOUR PROFILE ® 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 ARTOURA® Breast Tissue Expanders and CONTOUR PROFILE ® Expanders are provided in the Instructions for Use (IFU) available online at www.mentorwwllc.com
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 systematic 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.
Caution: US law restricts this device to sale by or on the order of a physician.

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.

The MENTOR ® Collection of Breast Implants are indicated for breast augmentation - in women who are at least 22 years old for MENTOR ® MemoryGel ® Breast Implants or MENTOR ® MemoryShape ® Breast Implants, and at least 18 years old for MENTOR ® Saline Breast Implants. MENTOR ® Breast Implants are also indicated for breast reconstruction.
Breast implant surgery should not be performed in women:
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.
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