Medical Device Manufacturer · US , Marlboro , NJ

Endooptiks, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1992

Total

Cleared

Denied

Endooptiks, Inc. has 5 FDA 510(k) cleared medical devices. Based in Marlboro, US.

Historical record: 5 cleared submissions from 1992 to 2009. Primary specialty: General & Plastic Surgery.

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

Endooptiks, 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 - Endooptiks, Inc.

5 devices

1-5 of 5