Osteogenics Biomedical, Inc.

Osteogenics Biomedical, Inc. — FDA 510(k) Submissions

Osteogenics Biomedical, Inc. has submitted 8 FDA 510(k) premarket notifications since 1999, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene, Barrier, Synthetic, Intraoral, Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction, Screw, Fixation, Intraosseous, Plate, Bone . Use the specialty filter in the sidebar to narrow results.