Medical Device Manufacturer · US , St. Paul , MN

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

3 submissions · 3 cleared · Since 2019

Total

Cleared

Denied

Vivaquant, Inc. has 3 FDA 510(k) cleared medical devices. Based in St. Paul, US.

Latest FDA clearance: Jul 2025. Active since 2019. Primary specialty: Cardiovascular.

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

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

3 devices

1-3 of 3