HomeUSAIds, Limited

Ids, Limited

USA · Indianapolis
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Brazil, Taiwan, Singapore, South Korea, Australia — 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
14listed device types
Class I 4Class II 10Class III 0
plus 13 registration records and 5 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
3registered devices
Class II 3
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
0active device licences
TWTaiwanTFDA
3valid device licences
Class I 1Class II 2
SGSingaporeHSA SMDR
1device registrations
CLASS C 1
KRSouth KoreaMFDS GMP
1GMP quality-system certificates
IVD import 1
AUAustraliaTGA ARTG
9active ARTG entries
IIa 1IIb 8
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 States13 registration records, 5 510(k), 0 PMA, 2 excluded
Brazil3 confirmed, 5 excluded
Manufacturer names merged into this page: IDS · IDS LTD · IDS SPA · IDS CO, LTD · IDS LTD.

Company information

Country
USA
City
Indianapolis

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

12017 · K171079
22018 · K181868
22023 · K233018

FDA listed device types

showing 8 of 14
Brush, Dermabrasion, Powered 1Otoscope 1Analyzer, Chemistry (Photometric, Discrete), For Clinical Use 1Heat Source For Bleaching Teeth 1Powered Light Based Non-Laser Surgical Instrument With Thermal Effect 1Vibrator For Climax Control Of Premature Ejaculation 1Ferritin, Antigen, Antiserum, Control 1Clinical Electronic Thermometer 1

Registration details (sample)

MarketIdentifierNameClass / date
USK233018PICOSECOND Nd:YAG Laser System2023-12-21
USK222485SMARTRION COMBI/Alexandrite & Long Pulsed Nd:YAG Laser2023-03-29
USK181868SHINY RPL System2018-10-05
BR80615950047IDS-iSYS DIRECT RENINClass II
BR80615950051IDS-iSYS Intact PTH CONTROLClass II
BR80615950050IDS-iSYS Intact PTHClass II

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