Medical Device Manufacturer · US , Doral , FL

American Medical Endoscopy, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2025

Total

Cleared

Denied

American Medical Endoscopy, Inc. has 3 FDA 510(k) cleared medical devices. Based in Doral, US.

Latest FDA clearance: Jun 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.

American Medical Endoscopy, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - American Medical Endoscopy, Inc.

3 devices

1-3 of 3

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: Jun 08, 2026