Inquis Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Inquis Medical - FDA 510(k) Cleared Devices
Recent clearances: Aventus Introducer Sheath, Aventus Thrombectomy System, Aventus Thrombectomy System
10
Total
10
Cleared
0
Denied
Inquis Medical has 10 FDA 510(k) cleared cardiovascular devices. Based in Redwood City, US.
Latest FDA clearance: Jul 2026. Active since 2023.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mojgan Saadat as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Inquis Medical
10 devices
Cleared
Jul 27, 2026
Powered Aventus Thrombectomy System™
Cardiovascular
115d
Cleared
Jul 15, 2026
Aventus Thrombectomy System
Cardiovascular
28d
Cleared
Apr 13, 2026
Aventus Introducer Sheath
Cardiovascular
91d
Cleared
Jan 15, 2026
Aventus Thrombectomy System
Cardiovascular
38d
Cleared
CT
Jun 13, 2025
Aventus Thrombectomy System
Cardiovascular
57d
Cleared
Mar 25, 2025
Aventus Thrombectomy System (IM-2100)
Cardiovascular
20d
Cleared
Feb 26, 2025
Aventus Thrombectomy System
Cardiovascular
33d
Cleared
May 14, 2024
Aventus Clot Management System
Cardiovascular
91d
Cleared
Mar 15, 2024
Aventus Thrombectomy System (IM-2001/IM-0002)
Cardiovascular
59d
Cleared
Nov 01, 2023
Aventus Thrombectomy System
Cardiovascular
55d