Inari Medical, Inc.
Inari Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2015, most recent 2026.
Top product codes for Inari Medical, Inc.
Recent clearances by Inari Medical, Inc.
- K262538 — Artix MT; Artix Thin-Walled Sheath
- K252508 — Intri26 Introducer Sheath
- K250421 — InThrill Thrombectomy System
- K250088 — FlowTriever2 Catheter
- K241894 — Artix MT; Artix Thin-Walled Thrombectomy Sheath
- K242557 — ClotTriever XL Catheter (41-102)
- K233069 — Removal System Large Bore 60 cc Syringe
- K234034 — VenaCore Thrombectomy Catheter (46-101)
- K233815 — ClotTriever Sheath
- K233646 — Intri24 Introducer Sheath (52-101)
- K231108 — Talon Transseptal Sheath
- K231848 — Triever20 Curve (21-201)
- K231782 — FlowSaver Blood Return System (80-101)
- K223210 — ClotTriever XL Catheter
- K230494 — ClotTriever BOLD Catheter
- K223613 — InThrill Thrombectomy System
- K223609 — RevCore Thrombectomy Catheter.
- K230331 — Protrieve Sheath
- K221483 — FlowSaver Blood Return System
- K221531 — ClotTriever Thrombectomy System
- K220415 — Protrieve Sheath
- K212392 — Intri24 Sheath
- K212632 — ClotTriever Thrombectomy System
- K210689 — ClotTriever Thrombectomy System
- K211013 — FlowTriever Retrieval/Aspiration System, FlowTriever Catheters, Triever 16, Triever 20, Triever 20 Curve, Triever 24
- K203333 — Triever20 Curve Catheter
- K181325 — FlowTriever Retrieval/Aspiration System
- K180466 — FlowTriever Retrieval/Aspiration System
- K180329 — ClotTriever Thrombectomy System
- K163549 — ClotTriever Thrombectomy System
- K143563 — Infusion Aspiration Catheter System
Data sourced from openFDA. This site is unofficial and independent of the FDA.