Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008717361

FEI Number

3008717361

Entity Name

QUALITY LIFE TECHNOLOGIES CO., LTD.

City/State/Country

Dongguan Guangdong, CN

Establishment Address

Building 1, No.8, Quling Middle Road, Liaobu Town, Dongguan City, Dongguan Guangdong 523425, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

QUALITY LIFE TECHNOLOGIES CO., LTD. (Owner Number: 10037536)

Owner / Operator Contact Address

Building 1, No.8, Quling Middle Road, Liaobu Town, Dongguan City, CN-GD 523425, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Wheelchair Curb Climber Powered Wheelchair Wheelchair Footrest Wheelchair Components Wheelchair Belt

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IMN	Climber, Curb, Wheelchair	Physical Medicine	Class 1	890.3920	2012-09-25
ITI	Wheelchair, Powered	Physical Medicine	Class 2	890.3860	2011-11-02
IMM	Footrest, Wheelchair	Physical Medicine	Class 1	890.3920	2012-09-25
KNN	Components, Wheelchair	Physical Medicine	Class 1	890.3920	2012-09-25
IQB	Belt, Wheelchair	Physical Medicine	Class 1	890.3920	2012-09-25

Official Correspondent

Hank Yang

US Agent Details

Christine Wang Email: Christinewang614@gmail.com Phone: (918) 9988916

Related Public Records

Same Entity

QUALITY LIFE TECHNOLOGIES CO., LTD.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K853594	Vessa , Ltd.	VESSA FLIVVA	1985-09-24
K142783	Heartway Medical Products Co., Ltd.	HEARTWAY Electrically Powered Wheelchair P27	2015-06-12

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0005-2018	Permobil, Ab Arvaltsvagen 10	2	Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR
Z-0006-2018	Permobil, Ab Arvaltsvagen 10	2	Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500
Z-0039-2007	Eagle Parts and Products	2	Eagle Parts and Products Model 624EZ Power Wheel Chairs with internally threaded wheel mount motors.
Z-0040-2007	Eagle Parts and Products	2	Eagle Parts and Products Model 624Mini Power Wheel Chairs with internally threaded wheel mount motors.

Similar Registrations

Registration Number	Establishment Name	Location
3008767869	METALFORM LTD	Dannevirke Hawke's Bay, NZ
3004473024	STEALTH PRODUCTS	BURNET, TX, US
3003636180	Chiaphua Components (Jiangxi) Limited	Yichun city Jiangxi, CN
3012411233	CHINA WONDERLAND NURSERYGOODS CO., LTD.	Dongguan City Guangdong, CN
8030931	PERMOBIL AB	Sundsvall Vasternorrland, SE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008717361. Last updated year: 2026. Please use registration number 3008717361 when referencing this establishment in official correspondence.