HomeUSADms-Service, LLC

Dms-Service, LLC

USA · Los Angeles
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Canada, Singapore, Australia, Hong Kong, Israel — 6 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
2listed device types
Class I 0Class II 2Class III 0
plus 4 registration records and 3 510(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
2active device licences
Class II 2
3 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
1device registrations
CLASS B 1
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
4active ARTG entries
Class I 2IIa 2
HKHong KongMDACS
1valid listings
Class II 1
ILIsraelAMAR
1registrations
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 States4 registration records, 3 510(k), 0 PMA, 8 excluded
Canada2 confirmed, 2 excluded
Manufacturer names merged into this page: dms-service llc · DMS HOLDINGS, INC. ATA BRIGGS MEDICAL SERVICE COMPANY · DMS-SERVICE LLC

Company information

Country
USA
City
Los Angeles

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

12013 · K131190
12016 · K160704
12017 · K163535

FDA listed device types

Electrode, Electrocardiograph 1Recorder, Magnetic Tape, Medical 1

Registration details (sample)

MarketIdentifierNameClass / date
USK163535my Patch sl2017-02-22
USK160704myPatch-s2016-07-15
USK131190MYPATCH2013-10-29
CA17816AMNIHOOK AMNIOTIC MEMBRANE PERFORATORClass II
CA86451HEALTHSMART BLOOD PRESSURE MONITORClass II

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