Last synced on 25 January 2026 at 3:41 am

DuraGraft

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN230002
510(k) Type
Direct
Applicant
Marizyme, Inc.
Country
United States
FDA Decision
Deleted
Decision Date
10/4/2023
Days to Decision
274 days

DuraGraft

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN230002
510(k) Type
Direct
Applicant
Marizyme, Inc.
Country
United States
FDA Decision
Deleted
Decision Date
10/4/2023
Days to Decision
274 days