Septodont

Septodont — FDA 510(k) Submissions

Septodont has submitted 9 FDA 510(k) premarket notifications since 2003, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Resin, Root Canal Filling, Material, Impression, Alloy, Amalgam, Bone Grafting Material, Synthetic, Cord, Retraction . Use the specialty filter in the sidebar to narrow results.