Medical Device Manufacturer · US , Safety Harbor , FL

Endo-Therapeutics, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1993

Total

Cleared

Denied

Endo-Therapeutics, Inc. has 7 FDA 510(k) cleared medical devices. Based in Safety Harbor, US.

Historical record: 7 cleared submissions from 1993 to 2009. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Endo-Therapeutics, Inc. Filter by specialty or product code using the sidebar.

Endo-Therapeutics, Inc. is one of 15071 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Endo-Therapeutics, Inc.

7 devices

1-7 of 7