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Leadoptik, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K251402LIA-1 Catheter (542-1)December 19, 2025
K251730LIA Console (542-7)December 19, 2025