Carwild Corp.

Carwild Corp. — FDA 510(k) Submissions

Carwild Corp. has submitted 6 FDA 510(k) premarket notifications since 1979, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Gauze/sponge, Internal, Gauze/sponge, Internal, X-ray Detectable, Dissector, Surgical, General & Plastic Surgery, Tape And Bandage, Adhesive . Use the specialty filter in the sidebar to narrow results.