Medical Device Manufacturer · US , Aliso Viejo , CA

Inari Medical, Inc. - FDA 510(k) Cleared Devices

32 submissions · 32 cleared · Since 2015

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
1-12 of 32
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