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/ Viatherm Therapeutics, LLC
Viatherm Therapeutics, LLC
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K250376
ViVY
November 5, 2025
K173300
ViaTherm BOOST
May 1, 2018