Dentatus USA , Ltd.

Dentatus USA , Ltd. — FDA 510(k) Submissions

Dentatus USA , Ltd. has submitted 4 FDA 510(k) premarket notifications since 1996, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Saw, Bone, Ac-powered, Resin, Denture, Relining, Repairing, Rebasing, Splint, Endodontic Stabilizing, Implant, Endosseous, Root-form . Use the specialty filter in the sidebar to narrow results.