Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003882673

FEI Number

3003882673

Entity Name

GLOBAL FABTECH WHEEL CHAIR (SHANGHAI) CO., LTD.

City/State/Country

SHANGHAI, CN

Establishment Address

No. 318 Tianfu Road, JIUTING, SONGJIANG, SHANGHAI 201615, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

GLOBAL FABTECH WHEEL CHAIR (SHANGHAI) CO., LTD. (Owner Number: 9043991)

Owner / Operator Contact Address

NO. 318 TIANFU ROAD, JIUTING, SONGJIANG, SHANGHAI, CN-NOTA 201615, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Zip'r Zip'r Mantis Zip'r Zip'r Fiji Sun Fluorescent Tanning Unit (FIJI Sun) Zip'r3 Xtra Zip'r3 Zip'r Zip'r PC Zip'r Mobility Zip'r Zip'r

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IMR	Device, Anti-Tip, Wheelchair	Physical Medicine	Class 1	890.3920	2012-09-10
ITI	Wheelchair, Powered	Physical Medicine	Class 2	890.3860	2011-03-01
IMP	Cushion, Wheelchair	Physical Medicine	Class 1	890.3920	2012-09-10
IMS	Support, Head And Trunk, Wheelchair	Physical Medicine	Class 1	890.3910	2012-09-10
LEJ	Booth, Sun Tan	General, Plastic Surgery	Class 2	878.4635	2018-12-21
INI	Vehicle, Motorized 3-Wheeled	Physical Medicine	Class 2	890.3800	2010-11-08
IML	Armrest, Wheelchair	Physical Medicine	Class 1	890.3920	2012-09-10
ITI	Wheelchair, Powered	Physical Medicine	Class 2	890.3860	2008-01-24
KNN	Components, Wheelchair	Physical Medicine	Class 1	890.3920	2012-09-10
INC	Cuff, Pusher, Wheelchair	Physical Medicine	Class 1	890.3910	2012-09-10

Official Correspondent

THOMAS TAN

US Agent Details

Zachary Tan Business: USA Email: zacharydtan@zipr.com Phone: (425) 6541097

Related Public Records

Same Entity

GLOBAL FABTECH WHEEL CHAIR (SHANGHAI) 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
K875190	Ultra Tan Intl. AB	ULTRA TAN PURPLE PRO	1988-01-14

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.
Z-0036-2007	Medline Industries Inc	2	Medline Strider Maxi 3 Scooter; a three wheeled battery operated scooter; manufactured by KYMCO, Kaohsiung, Taiwan for Medline Industries, Inc., One Medline Place, Mundelein, IL 60060 USA; model MDS807600 - red and MDS807600B - blue

Similar Registrations

Registration Number	Establishment Name	Location
3033506545	PHILIPCARE MEDICAL MANUFACTURING INC.	Lipa Batangas, PH
3004496806	HL CORP. (SHENZHEN)	BAOAN DISTRICT, SHENZHEN Guangdong, CN
3007728095	VISCOUNT HI-TECH (HUIZHOU) CO., LTD.	Huizhou Guangdong, CN
3004473024	STEALTH PRODUCTS	BURNET, TX, US
3016678950	Zhejiang Mateside Medical Devices Technology Co., Ltd	Ningbo Zhejiang, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003882673. Last updated year: 2026. Please use registration number 3003882673 when referencing this establishment in official correspondence.