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Bonvadis®

Page Type
Cleared 510(K)
510(k) Number
K232655
510(k) Type
Traditional
Applicant
StemCyte Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2024
Days to Decision
265 days
Submission Type
Summary

Bonvadis®

Page Type
Cleared 510(K)
510(k) Number
K232655
510(k) Type
Traditional
Applicant
StemCyte Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2024
Days to Decision
265 days
Submission Type
Summary