Medical Device Manufacturer · US , Santa Clara , CA

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

3 submissions · 3 cleared · Since 2017

Total

Cleared

Denied

VivaLNK, Inc. has 3 FDA 510(k) cleared medical devices. Based in Santa Clara, US.

Historical record: 3 cleared submissions from 2017 to 2020. Primary specialty: General Hospital.

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

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

3 devices

1-3 of 3