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/ Snucone Co., Ltd.
Snucone Co., Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K222792
SNUCONE Tissue Level Implant System
June 8, 2023
K210354
SNUCONE Bone Level Implant System
July 13, 2022