Vivaquant, Inc. Dba Rhythm Express is one of 16353 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vivaquant, Inc. Dba Rhythm Express - FDA 510(k) Cleared Devices
Recent clearances: RX-1 Sleep
1
Total
1
Cleared
0
Denied
Vivaquant, Inc. Dba Rhythm Express has 1 FDA 510(k) cleared medical devices. Based in Arden Hills, US.
Latest FDA clearance: Jun 2026. Active since 2026. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Vivaquant, Inc. Dba Rhythm Express Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by DuVal & Associates, P.A. as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Vivaquant, Inc. Dba Rhythm Express
1 devices