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Breast-Med, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K251989VizMark Preloaded Tissue Marker Device (VM-0001)December 12, 2025
K133697BREAST-MED TISSUE MARKERApril 10, 2015