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Hebei Healthplus Medical Device Co Ltd: FDA-registered device maker in Handan city Hebei, China, 1 510(k) clearance

Name: Hebei Healthplus Medical Device Co Ltd FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Hebei Healthplus Medical Device Co Ltd is registered with the FDA (registration 3007518294) in Handan city Hebei, China. It lists 18 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 1, 2007. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number: 3007518294
Address: No. 1, Chuangye Street, Southwest Industrial District Matou Ecological Industry Park, Handan city Hebei, China, 056046
Owner or operator: HEBEI HEALTHPLUS MEDICAL DEVICE CO LTD (10028061)
Roles: Manufacturer
First device listed: December 26, 2008
Registered through: 2026
Brand names listed: ACCESSORIES, WHEELCHAIR, ADAPTOR, HOLDER, SYRINGE, ADAPTOR, HYGIENE, BED, MANUAL, BED, PATIENT ROTATION, MANUAL, CANE, CART, EMERGENCY, CARDIOPULMONARY (EXCLUDING EQUIPMENT), CHAIR AND TABLE, MEDICAL and more

Devices it lists

Device	Product code	Class	Role	Source
Accessories, Wheelchair	KNO	1	Manufacturer	accessdata.fda.gov
Adaptor, Holder, Syringe	IQG	1	Manufacturer	accessdata.fda.gov
Adaptor, Hygiene	ILS	1	Manufacturer	accessdata.fda.gov
Bed, Manual	FNJ	1	Manufacturer	accessdata.fda.gov
Bed, Patient Rotation, Manual	INY	1	Manufacturer	accessdata.fda.gov
Cane	IPS	1	Manufacturer	accessdata.fda.gov
Cart, Emergency, Cardiopulmonary (Excluding Equipment)	BZN	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
Monitor, Bed Patient	KMI	1	Manufacturer	accessdata.fda.gov
Scale, Platform, Wheelchair	INF	1	Manufacturer	accessdata.fda.gov
Stand, Infusion	FOX	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
Walker, Mechanical, Poly Vinyl Chloride (Pvc)	NXE	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
March 1, 2007	K070176	MAXHEALTH MECHANICAL WHEELCHAIR, K1	IOR	Substantially Equivalent	Maxhealth Corp.	accessdata.fda.gov

Compare with other makers

Updated March 1, 2007. 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.