HomeSingaporeNsp Tech Pte, Ltd.

Nsp Tech Pte, Ltd.

Singapore · Singapore Central Singapore
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Singapore, Australia, Hong Kong — 4 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
4listed device types
Class I 1Class II 3Class III 0
plus 8 registration records and 5 510(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
0active device licences
TWTaiwanTFDA
0valid device licences
SGSingaporeHSA SMDR
3device registrations
CLASS B 3
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
1active ARTG entries
IIa 1
HKHong KongMDACS
1valid listings
Class II 1
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 States8 registration records, 5 510(k), 0 PMA, 1 excluded
Manufacturer names merged into this page: NSP TECH PTE LTD

Company information

Country
Singapore
City
Singapore Central Singapore

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

22019 · K181754
12020 · K193074
22022 · K221783

FDA listed device types

Tubes, Vials, Systems, Serum Separators, Blood Collection 1Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature 1Blood Specimen Collection Convenience Kit (Excludes Hiv) 1Kit, Screening, Urine 1

Registration details (sample)

MarketIdentifierNameClass / date
USK221783SafetiCET Safety Lancet2022-10-24
USK221604SafetiHeel, MediHeel, Novaplus2022-08-22
USK193074Bevel Up Holder2020-04-21

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