Aventus Thrombectomy System
FDA 510(k) K262030 · Inquis Medical
510(k) numberK262030
Submission
- Device name
- Aventus Thrombectomy System
- Applicant
- Inquis Medical
Menlo Park, CA, US - Received
- June 17, 2026
- Decision date
- July 15, 2026
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- QEZ – Aspiration Thrombectomy Catheter
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.5150
- Specialty
- Cardiovascular
To remove thrombus from the peripheral and/or coronary vasculature through aspiration.
Other 510(k)s with product code QEZ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K254035 | Mayumi Thrombectomy SystemQEZ · Traditional | MicroVention, Inc., d/b/a Terumo Neuro | 09/03/2026SE |
| K261105 | Powered Aventus Thrombectomy SystemQEZ · Traditional | Inquis Medical | 07/27/2026SE |
| K253589 | Liberant RX Aspiration CatheterQEZ · Traditional | Medtronic Interventional Vascular, Inc. | 04/23/2026SE |
| K254208 | FLOWRUNNER Aspiration SystemQEZ · Special | Expanse Medical, Inc. | 03/20/2026SE |
| K253925 | Aventus Thrombectomy SystemQEZ · Traditional | Inquis Medical | 01/15/2026SE |
| K252509 | AlphaVac Multipurpose Mechanical Aspiration System F1885QEZ · Traditional | AngioDynamics, Inc. | 11/24/2025SE |
| K251312 | Vesalio Peripheral SystemQEZ · Traditional | Vesalio, Inc. | 10/24/2025SE |
| K251488 | FLOWRUNNER Aspiration SystemQEZ · Special | Expanse Medical, Inc. | 07/14/2025SE |
| K243549 | JETi Hydrodynamic Thrombectomy SystemQEZ · Traditional | Abbott Medical | 04/04/2025SE |
| K250013 | VentiV 7Fr -12Fr MP Mechanical Thrombectomy System (VS7-MP60S, VS7-MP90S, VS8-MP60S…QEZ · Special | Control Medical Technology, Inc. / Dba Ventiv… | 03/24/2025SE |
More from Control Medical Technology, Inc. / Dba Ventiv Scientific
| 510(k) | Device | Decision |
|---|---|---|
| K261105 | Powered Aventus Thrombectomy SystemQEZ · Traditional | 07/27/2026SE |
| K260091 | Aventus Introducer SheathDYB · Traditional | 04/13/2026SE |
| K253925 | Aventus Thrombectomy SystemQEZ · Traditional | 01/15/2026SE |
| K251189 | Aventus Thrombectomy SystemQEW · Traditional | 06/13/2025SE |
| K250668 | Aventus Thrombectomy System (IM-2100)QEW · Special | 03/25/2025SE |
| K250202 | Aventus Thrombectomy SystemQEW · Special | 02/26/2025SE |
| K240426 | Aventus Clot Management SystemCAC · Traditional | 05/14/2024SE |
| K240117 | Aventus Thrombectomy System (IM-2001/IM-0002)QEW · Traditional | 03/15/2024SE |
| K232730 | Aventus Thrombectomy SystemQEW · Traditional | 11/01/2023SE |
Questions and answers
When was Aventus Thrombectomy System cleared by the FDA?
Aventus Thrombectomy System (K262030) received a 510(k) decision of Substantially Equivalent on July 15, 2026, 28 days after the submission was received.
What is the product code of K262030?
The FDA product code is QEZ – Aspiration Thrombectomy Catheter, a Class II (moderate risk) device regulated under 21 CFR 870.5150.