Endosee Corp is one of 19082 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Endosee Corp - FDA 510(k) Cleared Devices
Recent clearances: ENDOSEE MODEL 8000 U-SCOPE
1
Total
1
Cleared
0
Denied
Endosee Corp has 1 FDA 510(k) cleared medical devices. Based in Los Altos, US.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Endosee Corp Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Endosee Corp
1 devices