Geistlich Pharma AG

Geistlich Pharma AG — FDA 510(k) Submissions

Geistlich Pharma AG has submitted 25 FDA 510(k) premarket notifications since 2011, of which 25 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Barrier, Animal Source, Intraoral, Bone Grafting Material, Animal Source, Wound Dressing With Animal-derived Material(s), Filler, Bone Void, Calcium Compound, Mesh, Surgical . Use the specialty filter in the sidebar to narrow results.