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Cerenovus, Inc.

USA · Irvine

✓ Record-verifiedregistrations found in 8 markets

This company has registrations in United States, Canada, Taiwan, Singapore, South Korea, Australia, Hong Kong, Israel — 8 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

14listed device types

Class I 0Class II 10Class III 3unclassified 1

plus 100 registration records and 10 510(k), 37 PMA

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

0registered devices

this export covers Class I / II only (the cadastro route)

SASaudi ArabiaSFDA

0registered imported devices

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

CACanadaMDALL

26active device licences

Class II 13Class III 5Class IV 8

58 including historic records

TWTaiwanTFDA

3valid device licences

Class III 3

SGSingaporeHSA SMDR

8device registrations

CLASS D 8

KRSouth KoreaMFDS GMP

3GMP quality-system certificates

Import 3

AUAustraliaTGA ARTG

1active ARTG entries

Class III 1

HKHong KongMDACS

4valid listings

Class IV 4

ILIsraelAMAR

3registrations

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 States100 registration records, 10 510(k), 37 PMA

Canada26 confirmed, 0 excluded

Manufacturer names merged into this page: Cerenovus, Inc. · CERENOVUS, INC.

FDA 510(k) clearances by year

32023 · K230726

42024 · K241221

12025 · K251828

22026 · K262419

FDA listed device types

showing 8 of 14

Catheter, Continuous Flush 1Guide, Wire, Catheter, Neurovasculature 1Wire, Guide, Catheter 1Catheter, Intravascular, Diagnostic 1Catheter, Thrombus Retriever 1Catheter, Percutaneous, Neurovasculature 1Device, Neurovascular Embolization 1Catheter, Intravascular Occluding, Temporary 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K262419	MICRUSFRAME (MFR100202); MICRUSFRAME (MFR100253); MICRUSFRAME (MFR100305); MICRUSFRAME (MFR100356); MICRUSFRAME (MFR100407); MICRUSFRAME (MFR100412); MICRUSFRAME (MFR100509); MICRUSFRAME (MFR100517); MICRUSFRAME (MFR100611); MICRUSFRAME (MFR100626); MICRUSFRAME (MFR100713); MICRUSFRAME (MFR100730); MICRUSFRAME (MFR100816); MICRUSFRAME (MFR100829); MICRUSFRAME (MFR140225); MICRUSFRAME (MFR140303); MICRUSFRAME (MFR140304); MICRUSFRAME (MFR140306); MICRUSFRAME (MFR140406); MICRUSFRAME (MF	2026-08-14
US	K262398	CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing set	2026-08-13
US	K251828	CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set	2025-08-22
CA	2695	CODMAN EXTERNAL DRAINAGE SYSTEM	Class IV
CA	2837	CODMAN SOF'WIRE CABLE SYSTEM	Class III
CA	7681	CODMAN ME2 (MICRO ENDOSCOPIC ELECTRODE)	Class II

Cerenovus, 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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