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Inari Medical, Inc.

USA · Irvine

✓ Record-verifiedregistrations found in 7 markets

This company has registrations in United States, Brazil, Canada, Singapore, Australia, Hong Kong, Israel — 7 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable

CNChinaNMPA

n/aThis registry lists domestic registrants only

EUEuropean UnionEUDAMED

pendingnot queried

USUnited StatesFDA openFDA

6listed device types

Class I 1Class II 5Class III 0

plus 24 registration records and 56 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

8registered devices

Class II 8

11 including historic records

SASaudi ArabiaSFDA

0registered imported devices

low-risk imported devices only; a 2023 snapshot, not updated since

CACanadaMDALL

0active device licences

7 including historic records

TWTaiwanTFDA

pendingnot queried

SGSingaporeHSA SMDR

2device registrations

CLASS B 1CLASS D 1

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

20active ARTG entries

Class I 7Class III 1IIa 11Class Is (sterile) 1

HKHong KongMDACS

6valid listings

Class II 4Class IV 2

ILIsraelAMAR

6registrations

RURussiaRoszdravnadzor

pendingnot queried

Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States24 registration records, 56 510(k), 0 PMA

Brazil8 confirmed, 0 excluded

Manufacturer names merged into this page: Inari Medical, Inc. · Inari Medical, Costa Rica S.A. · INARI MEDICAL, INC.

FDA 510(k) clearances by year

22015

12016

22017

82018

42019

42020

52021

62022

162023

42024

42025

FDA listed device types

Catheter, Continuous Flush 1Peripheral Mechanical Thrombectomy With Aspiration 1Apparatus, Autotransfusion 1Catheter, Percutaneous 1Introducer, Catheter 1Retention Device, Suture 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K252508	Intri26 Introducer Sheath	2025-12-17
US	K253323	Protrieve Sheath	2025-10-29
US	K250421	InThrill Thrombectomy System	2025-05-12
BR	82968079001	Cateter de Trombectomia VenaCore	Class II
BR	80102519154	Sistema de Trombectomia ClotTriever	Class II
BR	82968079002	Sistema de Trombectomia Artix	Class II

Inari Medical, Inc.

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

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