HomeChinaSHENZHEN TPH TECHNOLOGY CO., LTD.

SHENZHEN TPH TECHNOLOGY CO., LTD.

China · Shenzhen
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Canada, Australia, Israel — 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
pendingnot queried
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
2listed device types
Class I 1Class II 1Class III 0
plus 25 registration records and 23 510(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
8 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
5active ARTG entries
IIa 5
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
4registrations
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 States25 registration records, 23 510(k), 0 PMA, 1 excluded
Manufacturer names merged into this page: SHENZHEN TPH TECHNOLOGY CO., LTD.

Company information

Country
China
City
Shenzhen

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

22022
22023
12024
112025 · K251754
72026 · K260259

FDA listed device types

Pump, Breast, Powered 1Catheters, Suction, Tracheobronchial 1

Registration details (sample)

MarketIdentifierNameClass / date
USK260259DiscreetDuo™ Flow Wearable Breast Pump (Model S3)2026-07-24
USK261199Wearable Breast Pump (Model S32A)2026-07-13
USK260864Mother's Nature W1 Warming Wearable Breast Pump2026-06-09

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