American Medical Endoscopy, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
American Medical Endoscopy, Inc. has 2 FDA 510(k) cleared medical devices. Based in Doral, US.
Latest FDA clearance: Mar 2026. Active since 2025. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by American Medical Endoscopy, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Medical Device Academy, Inc. and Shaily Shah.
2 devices