Collagen Matrix, Inc.

Collagen Matrix, Inc. — FDA 510(k) Submissions

Collagen Matrix, Inc. has submitted 47 FDA 510(k) premarket notifications since 2001, of which 47 received clearance as substantially equivalent to a predicate device.

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