Inari Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Inari Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Intri26 Introducer Sheath, InThrill™ Thrombectomy System, FlowTriever2 Catheter
30
Total
30
Cleared
0
Denied
Inari Medical, Inc. has 30 FDA 510(k) cleared cardiovascular devices. Based in Aliso Viejo, US.
Latest FDA clearance: Dec 2025. Active since 2015.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
3 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Inari Medical, Inc.
30 devices
Cleared
Dec 17, 2025
Intri26 Introducer Sheath
Cardiovascular
131d
Cleared
May 12, 2025
InThrill™ Thrombectomy System
Cardiovascular
88d
Cleared
CT
Mar 13, 2025
FlowTriever2 Catheter
Cardiovascular
58d
Cleared
Oct 15, 2024
Artix™ MT
Cardiovascular
109d
Cleared
Sep 27, 2024
ClotTriever XL Catheter (41-102)
Cardiovascular
30d
Cleared
Mar 26, 2024
Removal System Large Bore 60 cc Syringe
General Hospital
182d
Cleared
Feb 09, 2024
VenaCore Thrombectomy Catheter (46-101)
Cardiovascular
51d
Cleared
Dec 18, 2023
ClotTriever Sheath
Cardiovascular
18d
Cleared
Dec 12, 2023
Intri24 Introducer Sheath (52-101)
Cardiovascular
28d
Cleared
Sep 27, 2023
Talon Transseptal Sheath
Cardiovascular
161d
Cleared
Jul 21, 2023
Triever20 Curve (21-201)
Cardiovascular
28d
Cleared
Jul 14, 2023
FlowSaver Blood Return System (80-101)
Cardiovascular
28d