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Unik Orthopedics, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
2
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K240327
UNIKO PointCloud Knee Instruments
June 27, 2024
K193312
UNIKO PointCloud Knee Instruments
August 12, 2020