Medical Device Manufacturer · US , Findley , MN

Vivoxid , Ltd. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2007

Total

Cleared

Denied

Vivoxid , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Findley, US.

Historical record: 3 cleared submissions from 2007 to 2008.

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

FDA 510(k) Regulatory Record - Vivoxid , Ltd.

3 devices

1-3 of 3