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Foundation Dermal Regeneration Scaffold (DRS) Solo

Page Type
Cleared 510(K)
510(k) Number
K231937
510(k) Type
Traditional
Applicant
Bionova Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2023
Days to Decision
136 days
Submission Type
Summary

Foundation Dermal Regeneration Scaffold (DRS) Solo

Page Type
Cleared 510(K)
510(k) Number
K231937
510(k) Type
Traditional
Applicant
Bionova Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2023
Days to Decision
136 days
Submission Type
Summary