Medical Device Manufacturer · US , Annapolis , MD

Viatherm Therapeutics, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2018
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
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All2 Physical Medicine 2