FDA Opthalmic Devices Panel Meeting

Medical Devices Advisory Committee
April 25, 2008
Gaithersburg, Maryland

On April 25, 2008 a group of patients and family members of patients made their voices heard, literally, at the FDA. Some of their stories were horrific. All of their stories revealed the devastating consequences they had suffered and continue to suffer from LASIK surgery. This, despite the fact that many of the patients had been told by their surgeons that their surgery was a success.

We urge all patients who have suffered poor outcomes to register your experience with the FDA. We encourage everyone to register as a member of LASIK Surgery Watch. It is our continued hope that the growing body of evidence regarding the consequences of LASIK will result in the action needed to address this important public health issue.

Summary Minutes — Medical Devices Advisory Committee »