E&D Dental Products, Inc.

E&D Dental Products, Inc. — FDA 510(k) Submissions

E&D Dental Products, Inc. has submitted 3 FDA 510(k) premarket notifications since 1991, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Handle, Instrument, Dental, Agent, Tooth Bonding, Resin, Material, Impression Tray, Resin . Use the specialty filter in the sidebar to narrow results.