HomeHong KongAllied Hill Enterprises, Ltd.

Allied Hill Enterprises, Ltd.

Hong Kong · Hong Kong
✓ Record-verifiedregistrations found in 1 markets

This company has registrations in United States — 1 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
8listed device types
Class I 6Class II 2Class III 0
plus 9 registration records and 1 510(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
pendingnot queried
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 States9 registration records, 1 510(k), 0 PMA, 22 excluded
Brazil0 confirmed, 8 excluded
Saudi Arabia0 confirmed, 5 excluded
Canada0 confirmed, 5 excluded
Manufacturer names merged into this page: Allied Hill Enterprises, Ltd.

Company information

Country
Hong Kong
City
Hong Kong

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

12009 · K091198

FDA listed device types

Syringe, Irrigating (Non Dental) 1Pump, Breast, Non-Powered 1Tip, Rubber, Oral Hygiene 1Ring, Teething, Non-Fluid Filled 1Shield, Nipple 1Apparatus, Suction, Single Patient Use, Portable, Nonpowered 1Pump, Breast, Powered 1Ring, Teething, Fluid-Filled 1

Registration details (sample)

MarketIdentifierNameClass / date
USK091198LIQUID FILLED RING TEETHER, MODEL 03807, LIQUID FILLED RING TEETHER, MODELS 1962005, 1962011, LIQUID FILLED TEETHING2009-12-07

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