Gunze Limited

Gunze Limited — FDA 510(k) Submissions

Gunze Limited has submitted 5 FDA 510(k) premarket notifications since 2013, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Wound Dressing With Animal-derived Material(s), Mesh, Surgical, Absorbable, Staple Line Reinforcement . Use the specialty filter in the sidebar to narrow results.