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Interactions as seen by an industry representative among the FDA, the ADA, and industry in preparing a restorative
1Dentsply International, York, PA 17404.
Journal of Public Health Dentistry
|January 1, 1992
Abstract:
The regulation of a restorative material in the international and the American markets is discussed. The 510(k) process of approval by the Food and Drug Administration allows marketing of safe, effective, and improved materials in the shortest time at the lowest cost. The American Dental Association contributes to developing consensus performance standards in the United States. Acceptance of International Standards Organization standards is discussed.