# Inquis Medical

- Location (FDA's records): Menlo Park, CA
- FDA decisions: 10 (2023–2026): 10 510(k) clearances
- Product codes: QEW (5), QEZ (3), DYB (1), CAC (1)
- 510(k) review time since 2016: median 56 days, against 78 for FDA's reviews in the same codes and years (7 of 10 faster)
- Predicates its devices cite: 10 (6 its own); citations of its devices by later devices: 6 (6 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Inari Medical, Inc.: 2 (https://510kreport.com/company/inari-medical)
- W. L. Gore & Associates, Inc.: 1 (https://510kreport.com/company/w-l-gore-associates)
- Innova Vascular, Inc.: 1 (https://510kreport.com/company/innova-vascular)

## Its most-cited devices
- K253925: Aventus Thrombectomy System (2026), cited by 2
- K240117: Aventus Thrombectomy System (IM-2001/IM-0002) (2024), cited by 1
- K251189: Aventus Thrombectomy System (2025), cited by 1
- K240426: Aventus Clot Management System (2024), cited by 1
- K250202: Aventus Thrombectomy System (2025), cited by 1

## Recent decisions
- K261105: Powered Aventus Thrombectomy System™ (Jul 27, 2026)
- K262030: Aventus Thrombectomy System (Jul 15, 2026)
- K260091: Aventus Introducer Sheath (Apr 13, 2026)
- K253925: Aventus Thrombectomy System (Jan 15, 2026)
- K251189: Aventus Thrombectomy System (Jun 13, 2025)
- K250668: Aventus Thrombectomy System (IM-2100) (Mar 25, 2025)
- K250202: Aventus Thrombectomy System (Feb 26, 2025)
- K240426: Aventus Clot Management System (May 14, 2024)

Source page: https://510kreport.com/company/inquis-medical