Inquis Medical

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253925Aventus Thrombectomy SystemJanuary 15, 2026
K251189Aventus Thrombectomy SystemJune 13, 2025
K250668Aventus Thrombectomy System (IM-2100)March 25, 2025
K250202Aventus Thrombectomy SystemFebruary 26, 2025
K240426Aventus Clot Management SystemMay 14, 2024
K240117Aventus Thrombectomy System (IM-2001/IM-0002)March 15, 2024
K232730Aventus Thrombectomy SystemNovember 1, 2023