Last synced on 25 January 2026 at 3:41 am

ViVY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250376
510(k) Type
Traditional
Applicant
Viatherm Therapeutics, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2025
Days to Decision
268 days
Submission Type
Summary

ViVY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250376
510(k) Type
Traditional
Applicant
Viatherm Therapeutics, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2025
Days to Decision
268 days
Submission Type
Summary