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.

FDA 510(k) cleared devices by Genicon, Inc.

6 devices

1-6 of 6