Viatherm Therapeutics, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Viatherm Therapeutics, LLC - FDA 510(k) Cleared Devices
Recent clearances: ViVY, ViaTherm BOOST
2
Total
2
Cleared
0
Denied
Viatherm Therapeutics, LLC has 2 FDA 510(k) cleared medical devices. Based in Annapolis, US.
Latest FDA clearance: Nov 2025. Active since 2018. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Viatherm Therapeutics, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Graematter, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Viatherm Therapeutics, LLC
2 devices