Inari Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Triever Duo Catheter, Artix™ MT, Intri26 Introducer Sheath
32
Total
32
Cleared
0
Denied
FDA 510(k) Regulatory Record - Inari Medical, Inc. Cardiovascular ✕
31 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
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