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Chungwoo 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
K233120
CWM-930S, FIXER DV9
May 23, 2024
K222709
Retraction, CWM-910T, APOLEX Tite
March 21, 2023