Data / Medical devices / United States / Inquis Medical, Inc.
Inquis Medical, Inc.: FDA-registered device maker in Menlo Park, CA, United States, 7 510(k) clearances
Inquis Medical, Inc. is registered with the FDA (registration 3031823122) in Menlo Park, CA, United States. It lists 5 device types. The FDA files 7 510(k) clearances under its listings, the newest dated July 27, 2026. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3031823122
- Address
- 1530 O'Brien Drive Suite A, Menlo Park, CA, United States, 94025
- Owner or operator
- Inquis Medical, Inc. (10091176)
- Roles
- Manufacturer
- First device listed
- July 17, 2024
- Registered through
- 2027
- Brand names listed
- Aventus Clot Management System, Aventus Introducer Sheath, Aventus Thrombectomy System, Powered Aventus Thrombectomy System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Autotransfusion | CAC | 2 | Manufacturer | accessdata.fda.gov |
| Aspiration Thrombectomy Catheter | QEZ | 2 | Manufacturer | accessdata.fda.gov |
| Catheter, Continuous Flush | KRA | 2 | Manufacturer | accessdata.fda.gov |
| Introducer, Catheter | DYB | 2 | Manufacturer | accessdata.fda.gov |
| Peripheral Mechanical Thrombectomy With Aspiration | QEW | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 27, 2026 | K261105 | Powered Aventus Thrombectomy System | QEZ | Substantially Equivalent | Inquis Medical | accessdata.fda.gov |
| July 15, 2026 | K262030 | Aventus Thrombectomy System | QEZ | Substantially Equivalent | Inquis Medical | accessdata.fda.gov |
| April 13, 2026 | K260091 | Aventus Introducer Sheath | DYB | Substantially Equivalent | Inquis Medical | accessdata.fda.gov |
| January 15, 2026 | K253925 | Aventus Thrombectomy System | QEZ | Substantially Equivalent | Inquis Medical | accessdata.fda.gov |
| June 13, 2025 | K251189 | Aventus Thrombectomy System | QEW | Substantially Equivalent | Inquis Medical | accessdata.fda.gov |
| May 14, 2024 | K240426 | Aventus Clot Management System | CAC | Substantially Equivalent | Inquis Medical | accessdata.fda.gov |
| March 15, 2024 | K240117 | Aventus Thrombectomy System (IM-2001/IM-0002) | QEW | Substantially Equivalent | Inquis Medical | accessdata.fda.gov |
Compare with other makers
- All makers of Introducer, Catheter
- All makers of Aspiration Thrombectomy Catheter
- All makers of Catheter, Continuous Flush
- All makers of Apparatus, Autotransfusion
- All makers of Peripheral Mechanical Thrombectomy With Aspiration
Updated July 27, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.