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Thirona BV
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K250766
LungQ 4
October 2, 2025
K232412
LungQ v3.0.0
January 8, 2024