Medical Device Manufacturer · US , Irvine , CA

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

2 submissions · 2 cleared · Since 2018

Total

Cleared

Denied

Viseon, Inc. has 2 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 2 cleared submissions from 2018 to 2019. Primary specialty: General & Plastic Surgery.

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

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

2 devices

1-2 of 2