HomeUSAAcutus Medical, Inc.

Acutus Medical, Inc.

USA · Carlsbad
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Canada, Taiwan, Australia, Hong Kong — 5 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
24510(k) clearances
Class I 0Class II 0Class III 0
plus 0 registration records and 24 510(k)
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
1active device licences
Class II 1
4 including historic records
TWTaiwanTFDA
6valid device licences
Class II 5Class III 1
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
6active ARTG entries
Class I 5Class III 1
HKHong KongMDACS
7valid listings
Class III 2Class IV 5
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 States0 registration records, 24 510(k), 0 PMA
Canada1 confirmed, 0 excluded
Manufacturer names merged into this page: ACUTUS MEDICAL, INC.

Company information

Country
USA
City
Carlsbad

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

32017
12018
42019
42020
42021
52022
32023

Registration details (sample)

MarketIdentifierNameClass / date
USK233691FlexCath Cross Transseptal Solution2023-12-17
USK231091AcQMap High Resolution Imaging and Mapping System2023-07-10
USK230606AcQMap® High Resolution Imaging and Mapping System2023-05-02
CA107428ACQGUIDE MAX STEERABLE SHEATHClass II

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