Company · US
Inquis Medical
FDA 510(k) clearances and medical device recalls filed under this name, 2023 to 2026. Name variants (Inc, Corp, punctuation) are merged.
10510(k) clearances (4 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jul 27, 2026 | K261105 | Powered Aventus Thrombectomy System™ Inquis Medical | QEZ |
| Jul 15, 2026 | K262030 | Aventus Thrombectomy System Inquis Medical | QEZ |
| Apr 13, 2026 | K260091 | Aventus Introducer Sheath Inquis Medical | DYB |
| Jan 15, 2026 | K253925 | Aventus Thrombectomy System Inquis Medical | QEZ |
| Jun 13, 2025 | K251189 | Aventus Thrombectomy System Inquis Medical | QEW |
| Mar 25, 2025 | K250668 | Aventus Thrombectomy System (IM-2100) Inquis Medical | QEW |
| Feb 26, 2025 | K250202 | Aventus Thrombectomy System Inquis Medical | QEW |
| May 14, 2024 | K240426 | Aventus Clot Management System Inquis Medical | CAC |
| Mar 15, 2024 | K240117 | Aventus Thrombectomy System (IM-2001/IM-0002) Inquis Medical | QEW |
| Nov 1, 2023 | K232730 | Aventus Thrombectomy System Inquis Medical | QEW |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||