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Home›China›SHENZHEN VIATOM TECHNOLOGY CO., LTD.

SHENZHEN VIATOM TECHNOLOGY CO., LTD.

China · Shenzhen
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Canada, Singapore, Australia, Israel — 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
pendingnot queried
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
9listed device types
Class I 0Class II 9Class III 0
plus 9 registration records and 6 510(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
10 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
5device registrations
CLASS B 5
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
11active ARTG entries
IIa 10IIb 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
3registrations
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 States9 registration records, 6 510(k), 0 PMA
Manufacturer names merged into this page: SHENZHEN VIATOM TECHNOLOGY CO., LTD. · SHENZHEN VIATOM TECHNOLOGY CO.,LTD
Same-named companies — This database also contains companies with near-identical names: Viatom Technology Co., Ltd.. Company name alone cannot separate their registrations, so the figures below may include either.

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

12015 · K150869
22019 · K191088
12020 · K193348
12022 · K203812
12025 · K242876

FDA listed device types

showing 8 of 9
Transducer, Ultrasonic, Diagnostic 1System, Imaging, Pulsed Echo, Ultrasonic 1System, Measurement, Blood-Pressure, Non-Invasive 1Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) 1System, Imaging, Pulsed Doppler, Ultrasonic 1Oximeter, Wellness 1Oximeter, Infrared, Sporting, Aviation 1Oximeter 1

Registration details (sample)

MarketIdentifierNameClass / date
USK242876Pulse Oximeter ( PO2, PO2A, PO2B)2025-02-28
USK203812Oxyfit Pulse Oximeter2022-11-08
USK193348Blood Pressure Monitor2020-06-25

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