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HOME CARE TECHNOLOGY CO., LTD.

Taiwan · Tainan City

✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Brazil, Canada, 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

27listed device types

Class I 18Class II 9Class III 0

plus 29 registration records and 4 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

1registered devices

Class I 1

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

6active device licences

Class II 6

7 including historic records

TWTaiwanTFDA

pendingnot queried

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

1active ARTG entries

IIa 1

HKHong KongMDACS

pendingnot queried

ILIsraelAMAR

1registrations

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 States29 registration records, 4 510(k), 0 PMA, 49 excluded

Brazil1 confirmed, 7 excluded

Saudi Arabia0 confirmed, 3 excluded

Canada6 confirmed, 3 excluded

Manufacturer names merged into this page: FOSHAN ANY HOME CARE MEDICAL TECHNOLOGY CO.,LTD. · HOME CARE TECHNOLOGY CO., LTD. · HOME CARE TECHNOLOGY CO., LTD

FDA 510(k) clearances by year

42003 · K023000

FDA listed device types

showing 8 of 27

Ophthalmoscope, Battery-Powered 1Bed, Pediatric Open Hospital 1Stimulator, Muscle, Powered 1Pad, Heating, Powered 1Media, Electroconductive 1Cable, Electrode 1Electrode, Cutaneous 1Bed, Ac-Powered Adjustable Hospital 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K023000	HOME CARE VARIOUS MODELS OF POWERED MUSCLE STIMULATOR, HT-329M SERIES	2003-10-29
US	K022998	HOME CARE VAREIOUS MODELS OF POWERED MUSCLE STIMULATOR, HT-311, HT-311N, HT-312	2003-05-20
US	K023001	HOME CARE VARIOUS MODELS OF POWERED MUSCLE STIMULATOR, HT-326L	2003-04-08
BR	10342880012	COMFORT THERAPY	Class I
CA	76587	ULTRASOUND AND MUSCLE STIMULATOR	Class II
CA	79750	TRANSCUTANEOUS ELECTRIC NERVE STIMULATORS (TENS)	Class II
CA	79944	ELECTRODE CABLES	Class II

HOME CARE TECHNOLOGY CO., LTD.

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

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