Inari Medical - FDA 510(k) Cleared Devices
Recent clearances: Protrieve Sheath, Artix BG, Triever16 Curve
26
Total
26
Cleared
0
Denied
FDA 510(k) Regulatory Record - Inari Medical Cardiovascular ✕
26 devices
Cleared
Oct 29, 2025
Protrieve Sheath
Cardiovascular
29d
Cleared
May 02, 2023
Artix BG
Cardiovascular
32d
Cleared
Mar 23, 2023
Triever16 Curve
Cardiovascular
133d
Cleared
Mar 02, 2023
Artix AX
Cardiovascular
108d
Cleared
Jan 11, 2023
Artix BG
Cardiovascular
105d
Cleared
Aug 04, 2022
Mini-ClotTriever Thrombectomy System
Cardiovascular
129d
Cleared
Jul 11, 2022
Artix Ballon Guiding Sheath
Cardiovascular
17d
Cleared
May 23, 2022
Triever24, Triever20
Cardiovascular
217d
Cleared
Mar 25, 2022
Artix Thrombectomy Device
Cardiovascular
23d
Cleared
Jul 22, 2021
FlowSaver Blood Filter
Cardiovascular
181d
Cleared
Feb 24, 2021
Triever Catheters
Cardiovascular
30d
Cleared
Dec 18, 2020
FlowTriever Retrieval/Aspiration System
Cardiovascular
122d