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Data / Medical devices / China / Zhejiang J&J Mobility Co., Ltd

Zhejiang J&J Mobility Co., Ltd: FDA-registered device maker in Jinhua City Zhejiang, China, 2 510(k) clearances

Zhejiang J&J Mobility Co., Ltd is registered with the FDA (registration 3033848621) in Jinhua City Zhejiang, China. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated March 20, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3033848621
Address
#18, Baiyang Street, Wuyi, Jinhua City Zhejiang, China, 321200
Owner or operator
ZheJiang J&J Mobility Co., Ltd (10091687)
Roles
Exporter to the US, Manufacturer
First device listed
October 24, 2024
Registered through
2026
Brand names listed
Electric wheelchair (JJW-7002, JJW-7003, JJW-7004), Power wheelchair

Devices it lists

DeviceProduct codeClassRoleSource
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
March 20, 2026K253849Electric wheelchair (JJW-7002, JJW-7003)ITISubstantially EquivalentZheJiang J&J Mobility Co., Ltd.accessdata.fda.gov
October 8, 2024K240563Power Wheelchair (JJW-6001)ITISubstantially EquivalentZheJiang J&J Mobility Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated March 20, 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.