Business · 10/10/2000Updated: 10/17/2026 · 1 min read
FDA Reclassifies Endosseous Dental Implant Accessories from Class III to Class I
Summary
The FDA is reclassifying endosseous dental implant accessories from Class III to Class I, exempting them from premarket notification, due to new information and amendments to the Federal Food, Drug, and Cosmetic Act, as well as the Medical Device Amendments of 1976 and the Safe Medical Devices Act of 1990.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →