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Some types of surgeries have their own unique risks associated with them and breast augmentation procedures are one of those types of surgeries.


One of the inherent risks associated with breast implant devices is the off chance that they will rupture their exterior shell and leak their liquid filler. That fluid can cause a number of health problems once it leaks into the human body. While most modern implants are designed with a two layer exterior shell Derwin James Chargers Jersey , leaks can and still do occur.


Traditional silicone gel implants and the saline solution implant will leak their liquid filler into the body should their exterior shell become ruptured. The leakage of silicone gel into the human body is allegedly linked to a number of serious health conditions, including death. The leakage of saline solution into the body is a virtually harmless condition; the saline solution poses no threat to the health and well-being of a human being.


There is a new breast implant device that has recently made its debut in the United States. This new implant device may be impervious to implant rupture and leakage, at least in the traditional sense. The official name for this medical device is the cohesive gel implant. However Derrius Guice Redskins Jersey , you’ve probably heard it by its common nickname: the Gummy Bear breast implant.


What makes the cohesive gel implant unique in design compared to other implant devices is its filler. The silicone gel inside its exterior shell is not in liquid form; it is one large, solid mass of gel that is preformed into the natural shape and slope of a real breast. If you’ve heard about the cohesive gel implant and you’re considering this type of implant for your breast augmentation surgery, you should know that the FDA currently restricts the implant from being used within the United States. The FDA only allows a select few women to have the implant device for their surgery. The restriction on the general use of the implant for augmentation surgeries is a result of the current clinical trial being performed on the device.


The FDA wants onl


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