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Neuravi Limited

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251789EMBOTRAP III Revascularization DeviceSeptember 25, 2025
K233924EMBOGUARD Balloon Guide CatheterApril 18, 2024
K212340EMBOGUARD Balloon Guide CatheterDecember 17, 2021