Medical Device Manufacturer · US , Winter Park , FL

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

6 submissions · 6 cleared · Since 2016

Total

Cleared

Denied

Genicon, Inc. has 6 FDA 510(k) cleared medical devices. Based in Winter Park, US.

Historical record: 6 cleared submissions from 2016 to 2019. Primary specialty: General & Plastic Surgery.

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

Genicon, 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 - Genicon, Inc.

6 devices

1-6 of 6