Medical Device Manufacturer · US , Los Angeles , CA

Cogent Light Technologies, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1994

Total

Cleared

Denied

Cogent Light Technologies, Inc. has 5 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Historical record: 5 cleared submissions from 1994 to 2000. Primary specialty: Gastroenterology & Urology.

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

Cogent Light Technologies, 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 - Cogent Light Technologies, Inc.

5 devices

1-5 of 5