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Sigmagraft, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
4
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K223912
InterCollagen® Guide
August 17, 2023
K221808
InterOss Collagen
March 18, 2023
K151209
InterOss
November 6, 2015