Inari Medical, Inc. is one of 25937 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: Triever Duo Catheter, Artix™ MT, Intri26 Introducer Sheath
32
Total
32
Cleared
0
Denied
Inari Medical, Inc. has 32 FDA 510(k) cleared cardiovascular devices. Based in Aliso Viejo, US.
Latest FDA clearance: Sep 2026. 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.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant. 3 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Inari Medical, Inc.
32 devices
Cleared
Sep 18, 2026
Triever Duo Catheter
Cardiovascular
352d
Cleared
Aug 21, 2026
Artix™ MT
Cardiovascular
29d
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