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Data / Medical devices / China / Yongkang Ruihe Metal Products Co.,ltd

Yongkang Ruihe Metal Products Co.,ltd: FDA-registered device maker in Yongkang Zhejiang, China, 4 510(k) clearances

Yongkang Ruihe Metal Products Co.,ltd is registered with the FDA (registration 3014983822) in Yongkang Zhejiang, China. It lists 3 device types. The FDA files 4 510(k) clearances under its listings, the newest dated July 7, 2026. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3014983822
Address
The 2nd Building, No.99, Huaxi Road, Xicheng Street, Yongkang City, Zhejiang Province., Yongkang Zhejiang, China, 321302
Owner or operator
YONGKANG RUIHE METAL PRODUCTS CO.,LTD (10089543)
Roles
Exporter to the US, Manufacturer
First device listed
December 15, 2023
Registered through
2026
Brand names listed
BATH LIFT, Electric Wheelchair, Electric Wheelchair (XW-LY007), JH-KN01, Knee Walker, Mobility Scooter (R200), Mode: RH05, R100 and more

Devices it lists

DeviceProduct codeClassRoleSource
Vehicle, Motorized 3-WheeledINI2Exporter to the US, Manufactureraccessdata.fda.gov
Walker, MechanicalITJ1Exporter to the US, Manufactureraccessdata.fda.gov
Wheelchair, PoweredITI2Exporter to the US, Manufactureraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
July 7, 2026K261164Electric wheelchair (XW-LY007 )ITISubstantially EquivalentYongkang Ruihe Metal Product Co., Ltd.accessdata.fda.gov
July 7, 2026K261163Mobility Scooter (R200)INISubstantially EquivalentYongkang Ruihe Metal Product Co., Ltd.accessdata.fda.gov
September 22, 2021K200423Electric Wheelchair (XW-LY001)ITISubstantially EquivalentYongkang Dingchang Industry & Trade Co., Ltd.accessdata.fda.gov
June 24, 2019K182411Scooter, Model: R-100INISubstantially EquivalentYongkang Dingchang Industry & Trade Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated July 7, 2026. 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.