Medical Device Manufacturer · US , Los Altos , CA

Endosee Corp - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2013

Recent clearances: ENDOSEE MODEL 8000 U-SCOPE

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Endosee Corp Obstetrics & Gynecology ✕

1 devices

1-1 of 1

Cleared Mar 08, 2013

ENDOSEE MODEL 8000 U-SCOPE

Obstetrics & Gynecology · 150d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 18, 2026