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FDA 510(k)

Aventus Thrombectomy System

K-Number: K262030 · 2026-07-15

Decision Date2026-07-15
Product CodeQEZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Aventus Thrombectomy System is the device name listed in this FDA 510(k) record. The listed applicant is Inquis Medical. It received FDA 510(k) clearance on 2026-07-15 under 510(k) number K262030. The device is classified under product code QEZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Aventus Thrombectomy System?

Aventus Thrombectomy System is a medical device that received FDA 510(k) clearance on 2026-07-15. The listed applicant is Inquis Medical. The 510(k) number is K262030.

When did Aventus Thrombectomy System receive FDA 510(k) clearance?

Aventus Thrombectomy System received FDA 510(k) clearance on 2026-07-15, under 510(k) number K262030.

Who is the listed applicant for Aventus Thrombectomy System?

The FDA 510(k) record lists Inquis Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Aventus Thrombectomy System?

The FDA product code for Aventus Thrombectomy System is QEZ.

Other records listing Inquis Medical as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 9 devices →

Related Devices (Code: QEZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.