Tri W-G, Inc.

Tri W-G, Inc. — FDA 510(k) Submissions

Tri W-G, Inc. has submitted 35 FDA 510(k) premarket notifications since 1979, of which 35 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Table, Powered, Table, Radiographic, Tilting, Exerciser, Powered, Bath, Paraffin, Exerciser, Measuring . Use the specialty filter in the sidebar to narrow results.