Friadent GmbH

Friadent GmbH — FDA 510(k) Submissions

Friadent GmbH has submitted 18 FDA 510(k) premarket notifications since 1999, of which 18 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Implant, Endosseous, Root-form, Bone Grafting Material, Synthetic, Handpiece, Rotary Bone Cutting . Use the specialty filter in the sidebar to narrow results.