Denver Splint Co.

Denver Splint Co. — FDA 510(k) Submissions

Denver Splint Co. has submitted 4 FDA 510(k) premarket notifications since 1993, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrosurgical, Cutting & Coagulation & Accessories, Balloon, Epistaxis, Applicator, Ent Drug, Tape And Bandage, Adhesive . Use the specialty filter in the sidebar to narrow results.