Seare Biomedical Corp.

Seare Biomedical Corp. — FDA 510(k) Submissions

Seare Biomedical Corp. has submitted 8 FDA 510(k) premarket notifications since 1998, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Implant, Muscle, Pectoralis, Elastomer, Silicone Block, Prosthesis, Chin, Internal, Prosthesis, Nose, Internal, Implant, Malar . Use the specialty filter in the sidebar to narrow results.