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Armis Biopharma, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K220759Armis VeriCyn Wound WashMay 25, 2023
K202777VeriFixx™ Small Bone ImplantNovember 17, 2020