The current scientific debate regarding the safety of amalgam dental restorations being conducted in the US is presented. The material is based on a meeting held on December 14 and 15, 2010 by the Dental Products Panel of the Medical Devices Advisory Committee of the Food and Drug Administration. The scientific and historic context of the debate is provided, followed by scientific arguments, public testimony and panel deliberations.
The FDA was charged with evaluating and classifying medical devices in 1976. Amalgam manufacturers have been able to successfully shirk the burden of proving safety, which should rightfully be assigned to them. If the FDA assigns the burden to prove harm to U.S. consumer groups, the FDA condemns itself to perpetual study and inaction. This will result in an ineffective agency and an unprotected public, devastated by preventable degenerative disease.
Dr Michael Margolis presents evidence to the FDA's dental products panel in 2010 that mercury from amalgam fillings is absorbed into the gum and jaw bone
When covering the 2010 FDA dental products panel hearing on the safety of dental amalgam fillings, the press widely promoted the "red herring" comment from FDA panelist, Susan Griffin (of the EPA). The comment was directed at the assertion that the Fawer study should not be relied on for the basis of a risk assessment because many of the workers in the study were also exposed to chlorine, which inhibits uptake of mercury (up to 40%).
At the end of the FDA dental products panel hearing to evaluate the safety of amalgam, FDA’s scientific panel, including neurologists, toxicologists, epidemiologists, and environmental health specialists concluded that, contrary to the claims of FDA’s in-house dentist Susan Runner, "amalgam is not safe for everybody." and to stop its use in susceptible, at risk populations.
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