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Mimedx Group, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
12
Compliance Actions
1
Recent 510(k) Clearances
K-Number
Device
Date
K100313
HYDROFIX SURGICAL SHEET
June 14, 2011
K111137
HYDROFIX VASO SHIELD
May 20, 2011
K101805
HYDROFIX VASO SHIELD
April 8, 2011
K101826
HYDROFIX VASO SHIELD, MODEL HVS-001-0610
July 28, 2010
K100905
HYDROFIX SURGICAL SHEET
June 2, 2010