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Double Care Medical Technology Co.,ltd.: FDA-registered device maker in Huizhou City Guangdong, China, 1 510(k) clearance

Name: Double Care Medical Technology Co.,ltd. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Double Care Medical Technology Co.,ltd. is registered with the FDA (registration 3043749706) in Huizhou City Guangdong, China. It lists 19 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 13, 1992. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3043749706
Address: 318 He'an Avenue Yuanzhou Town, Boluo County, Huizhou City Guangdong, China, 0
Owner or operator: DOUBLE CARE MEDICAL TECHNOLOGY CO.,LTD. (10038725)
Roles: Manufacturer
First device listed: November 7, 2011
Registered through: 2026
Brand names listed: ALEX ORTHOPEDIC, INC., Bath bench, Bath rail, Bathtub Rail, Bed rail, CPR mask, Cane, Commode and more

Devices it lists

Device	Product code	Class	Role	Source
Accessory, Surgical Apparel	LYU	1	Manufacturer	accessdata.fda.gov
Adaptor, Hygiene	ILS	1	Manufacturer	accessdata.fda.gov
Aid, Transfer	IKX	1	Manufacturer	accessdata.fda.gov
Bed, Manual	FNJ	1	Manufacturer	accessdata.fda.gov
Cane	IPS	1	Manufacturer	accessdata.fda.gov
Cap, Surgical	FYF	1	Manufacturer	accessdata.fda.gov
Chair And Table, Medical	KMN	1	Manufacturer	accessdata.fda.gov
Chair, With Casters	INM	1	Manufacturer	accessdata.fda.gov
Crutch	IPR	1	Manufacturer	accessdata.fda.gov
Exerciser, Non-Measuring	ION	1	Manufacturer	accessdata.fda.gov
Mask, Oxygen	BYG	1	Manufacturer	accessdata.fda.gov
Non-Surgical Gown	OEA	1	Manufacturer	accessdata.fda.gov
Orthosis, Limb Brace	IQI	1	Manufacturer	accessdata.fda.gov
Pack, Hot Or Cold, Reusable	IME	1	Manufacturer	accessdata.fda.gov
Stand, Infusion	FOX	1	Manufacturer	accessdata.fda.gov
Stocking, Medical Support (For General Medical Purposes)	FQL	1	Manufacturer	accessdata.fda.gov
Tips And Pads, Cane, Crutch And Walker	INP	1	Manufacturer	accessdata.fda.gov
Walker, Mechanical	ITJ	1	Manufacturer	accessdata.fda.gov
Wheelchair, Mechanical	IOR	1	Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
January 13, 1992	K915262	BANTEX BRAND WHEELCHAIRS	IOR	Substantially Equivalent	Bantex Corp.	accessdata.fda.gov

Compare with other makers

Updated January 13, 1992. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.