Edward Weck, Inc.

Edward Weck, Inc. — FDA 510(k) Submissions

Edward Weck, Inc. has submitted 140 FDA 510(k) premarket notifications since 1976, of which 140 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Forceps, Ophthalmic, Electrosurgical, Cutting & Coagulation & Accessories, Clip, Implantable, Cutter, Surgical, Clamp, Surgical, General & Plastic Surgery . Use the specialty filter in the sidebar to narrow results.