i-Cut
Apr 2025
134d
A.M.I. Agency For Medical Innovations GmbH
1
Total
1
Cleared
0
Denied
A.M.I. Agency For Medical Innovations GmbH — FDA 510(k) Submissions
A.M.I. Agency For Medical Innovations GmbH has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Laparoscope, Gynecologic (and Accessories) . Use the specialty filter in the sidebar to narrow results.
1 devices