Med-Tool, Inc.

Med-Tool, Inc. — FDA 510(k) Submissions

Med-Tool, Inc. has submitted 28 FDA 510(k) premarket notifications since 1984, of which 28 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Pliers, Surgical, Punch, Surgical, Wrench, Vise, Bench, Surgical, Clamp . Use the specialty filter in the sidebar to narrow results.