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Medifun Corporation

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K241750Medifun Safety Lancet ( MSL1 series)August 15, 2024
K231797Medifun Lancing Device, Model No. LD-E1November 22, 2023