Sunday, August 2, 2009

FDA Classification Disaster

IAOMT Response
On Tuesday, July 28, 2009, the FDA completed its classification of the traditional dental amalgam filling material by making it a Class II device, with minimal controls. Dr. Susan Runner, the acting director of the dental devices division, stated flatly that there are no serious concerns about the toxic mercury exposure from amalgam, that is in fact thoroughly documented in the scientific literature.