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Vesalio

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251097V-DAC CatheterJanuary 6, 2026
K253407NeVa PV Thrombectomy DeviceNovember 24, 2025
K251006NeVasc Aspiration SystemNovember 10, 2025
K251312Vesalio Peripheral SystemOctober 24, 2025
K201085NeVa PV Thrombectomy DeviceJanuary 15, 2021