Prosidyan, Inc.

Prosidyan, Inc. — FDA 510(k) Submissions

Prosidyan, Inc. has submitted 12 FDA 510(k) premarket notifications since 2014, of which 12 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Filler, Bone Void, Calcium Compound, Syringe, Piston . Use the specialty filter in the sidebar to narrow results.