Medical Device Manufacturer · US , College Park , MD

Gel-E, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2018

Total

Cleared

Denied

Gel-E, Inc. has 3 FDA 510(k) cleared medical devices. Based in College Park, US.

Historical record: 3 cleared submissions from 2018 to 2019. Primary specialty: General & Plastic Surgery.

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

Gel-E, 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 - Gel-E, Inc.

3 devices

1-3 of 3