Conmed Corporation

Conmed Corporation — FDA 510(k) Submissions

Conmed Corporation has submitted 82 FDA 510(k) premarket notifications since 2004, of which 82 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrosurgical, Cutting & Coagulation & Accessories, Fastener, Fixation, Nondegradable, Soft Tissue, Laparoscope, General & Plastic Surgery, Fastener, Fixation, Biodegradable, Soft Tissue, Sterilization Wrap Containers, Trays, Cassettes & Other Accessories . Use the specialty filter in the sidebar to narrow results.