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MicroVention, Inc.

USA · Aliso Viejo

✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Brazil, Canada — 3 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

23listed device types

Class I 0Class II 17Class III 5unclassified 1

plus 80 registration records and 86 510(k), 50 PMA

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

0registered devices

1 including historic records

SASaudi ArabiaSFDA

0registered imported devices

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

CACanadaMDALL

1active device licences

Class II 1

29 including historic records

TWTaiwanTFDA

pendingnot queried

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

pendingnot queried

HKHong KongMDACS

pendingnot queried

ILIsraelAMAR

pendingnot queried

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 States80 registration records, 86 510(k), 50 PMA, 4 excluded

Brazil0 confirmed, 3 excluded

Canada1 confirmed, 0 excluded

Manufacturer names merged into this page: MicroVention, Inc. · MICROVENTION, INC. · MICROVENTION, INC

FDA 510(k) clearances by year

12004

12005

12007

62008

92009

62010

82011

82012

72013

22014

62015

52016

22017

22018

32019

52020

32022

32023

12024

12025

FDA listed device types

showing 8 of 23

Agents, Embolic, For Treatment Of Uterine Fibroids 1Catheter, Continuous Flush 1Guide, Wire, Catheter, Neurovasculature 1Apparatus, Suction, Ward Use, Portable, Ac-Powered 1Wire, Guide, Catheter 1Tube, Aspirating, Flexible, Connecting 1Catheter, Intravascular, Diagnostic 1Syringe, Piston 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K243638	MV Flow Aspiration Pump (MVFLOWPMP01)	2025-06-13
US	K232542	Wedge XL Delivery Catheter	2024-05-16
US	K230775	SOFIA EX Intracranial Support Catheter	2023-09-14
CA	61572	HYDROLINK SYRINGE KIT	Class II

MicroVention, 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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