Vivaquant, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vivaquant, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Rhythm Express Remote Cardiac Monitoring System (RX-1 mini), RX-1 Rhythm Express Remote Cardiac Monitoring System, RX-1 Rhythm Express Remote Cardiac Monitoring System
3
Total
3
Cleared
0
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.
Regulatory submissions have been managed by Regulatory Technology Services, LLC, Borderless Compliance, LLC and DuVal & Associates, P.A..
FDA 510(k) Regulatory Record - Vivaquant, Inc.
3 devices