# K253925: Aventus Thrombectomy System

- Pathway: 510(k) (Traditional)
- Applicant: Inquis Medical
- Decided: Jan 15, 2026 after 38 days
- Product code: QEZ (Aspiration Thrombectomy Catheter)
- Device class: 2
- Regulation: 21 CFR 870.5150
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K951592 (1996). 11 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K251189: Aventus Thrombectomy System, Inquis Medical (2025) Summary page 5.
- K240426: Aventus Clot Management System, Inquis Medical (2024) Summary page 5.

## Most influential descendants
- K261105: Powered Aventus Thrombectomy System™ (2026), 0 descendants of its own
- K262030: Aventus Thrombectomy System (2026), 0 descendants of its own

## Indications for use
The Aventus Thrombectomy System is indicated for: • The non-surgical removal of emboli and thrombi from blood vessels. • Injection, infusion, and/or aspiration of contrast media and other fluids into or from a blood vessel. The Aventus Thrombectomy System is intended for use in the peripheral vasculature and for the treatment of pulmonary embolism.

Source page: https://510kreport.com/device/K253925
Methodology: https://510kreport.com/methodology