Data / Medical devices / China / Caremax Rehabilitation Equipment Co., Ltd.

Caremax Rehabilitation Equipment Co., Ltd.: FDA-registered device maker in Foshan City Guangdong, China, 1 510(k) clearance

Name: Caremax Rehabilitation Equipment Co., Ltd. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Caremax Rehabilitation Equipment Co., Ltd. is registered with the FDA (registration 3005555653) in Foshan City Guangdong, China. It lists 16 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: 3005555653
Address: Pingnan Industrial Area, Shugang Dadao Pingzhou Town, Nanhai Area, Foshan City Guangdong, China, 528251
Owner or operator: CAREMAX REHABILITATION EQUIPMENT CO., LTD. (9082081)
Roles: Exporter to the US, Manufacturer
First device listed: January 23, 2006
Registered through: 2026
Brand names listed: #XLWM-KS, AF-005A, ALEX ORTHOPEDIC, INC, Bath Bench, Bath Rail, Bed Rail, C-200, C-300 and more

Devices it lists

Device	Product code	Class	Role	Source
Adaptor, Hygiene	ILS	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Aid, Transfer	IKX	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Bed, Manual	FNJ	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Cane	IPS	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Chair And Table, Medical	KMN	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Chair, With Casters	INM	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Crutch	IPR	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Exerciser, Non-Measuring	ION	1	Exporter to the US, Manufacturer	accessdata.fda.gov
First Aid Kit Without Drug	OHO	1	Manufacturer	accessdata.fda.gov
Mask, Oxygen	BYG	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Pack, Hot Or Cold, Reusable	IME	1	Manufacturer	accessdata.fda.gov
Stand, Infusion	FOX	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Stocking, Medical Support (For General Medical Purposes)	FQL	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Tips And Pads, Cane, Crutch And Walker	INP	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Walker, Mechanical	ITJ	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Wheelchair, Mechanical	IOR	1	Exporter to the US, 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.