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/ Biocore9, LLC
Biocore9, LLC
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K212761
Biocore9 Acetabular Cup System
May 17, 2022
K201219
Biocore9 Femoral Head Resurfacing Component
January 19, 2021
K193122
Biocore9 Humeral Resurfacing System
May 15, 2020