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Leo Medical Co., Ltd.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K241888Single-use Balloon Dilatation CatheterDecember 20, 2024
K172985Ligation DeviceJune 14, 2018