The FDA Approval of Silicone Breast Implants 

The big story in cosmetic surgery today is the FDA’s approval of Silicone Breast Implants after they were pulled from the market 14 years ago.  Both the American Society for Aesthetic Plastic Surgery (ASAPS) and The American Society of Plastic Surgeons (ASPS), the two largest and most respected plastic surgery membership organizations, applauded the FDA’s decision.

There are two manufactures who received an “approval by conditions” letter by the FDA, Allergan Corporation and Mentor Corporation.  Both companies have been conducting long-term trials to prove the safety and effectiveness of silicone gel-filled implants.  The “approval by conditions” means the implants were FDA approved on the condition that Allergan and Mentor meet several requirements including continuing their implant study through the next 10 years (see www.breastimplantsafety.org/ImplantOptions/trials.php for more about these and other FDA conditions).

ASPS statistics page shows 383,886 women elected to have a breast augmentation procedure 2006.  The addition of silicon implants will give women more choices over what goes into their body.  When considering the Breast Augmentation or Breast Reconstruction procedures, be sure to ask you surgeon about the differences between saline and silicone so that you may make a well informed decision.  ASPS and ASAPS have set up a joint website to help the public understand their choices and make a better informed decision, www.breastimplantsafety.org.   

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For additional information on this Silincone Breast Implants article, please contact:

Jeremy Hartling
(713) 799-9999

Source: Jeremy Hartling

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