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Home›China›ZHEJIANG INNUOVO REHABILITATION DEVICES CO., LTD.

ZHEJIANG INNUOVO REHABILITATION DEVICES CO., LTD.

China · Dongyang Zhejiang
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Australia — 2 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
4listed device types
Class I 2Class II 2Class III 0
plus 22 registration records and 20 510(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
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
8active ARTG entries
Class I 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 States22 registration records, 20 510(k), 0 PMA
Manufacturer names merged into this page: ZHEJIANG INNUOVO REHABILITATION DEVICES CO., LTD.

Company information

Country
China
City
Dongyang Zhejiang

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

62022
42023
52024 · K242471
52026 · K260094

FDA listed device types

Vehicle, Motorized 3-Wheeled 1Wheelchair, Powered 1Walker, Mechanical 1Components, Wheelchair 1

Registration details (sample)

MarketIdentifierNameClass / date
USK260094Mobility Scooter (W3465, W3902 (S50 Carbon))2026-08-10
USK260176Mobility Scooter (W3483, W3483A)2026-08-10
USK253812Power Wheelchair (W5915B, W5915C, W5915D)2026-06-18

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