Agency For Medical Innovations GmbH

Agency For Medical Innovations GmbH — FDA 510(k) Submissions

Agency For Medical Innovations GmbH has submitted 4 FDA 510(k) premarket notifications since 2015, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Containment System, Laparoscopic Power Morcellation, With Instrument Port, Ligator, Hemorrhoidal, Electrosurgical, Cutting & Coagulation & Accessories, Surgical Instruments, G-u, Manual (and Accessories) . Use the specialty filter in the sidebar to narrow results.