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Data / Medical devices / China / Zhejiang Jianrui Technology Co., Ltd

Zhejiang Jianrui Technology Co., Ltd: FDA-registered device maker in Jinhua City Zhejiang, China, 1 510(k) clearance

Zhejiang Jianrui Technology Co., Ltd is registered with the FDA (registration 3033796886) in Jinhua City Zhejiang, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 7, 2024. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3033796886
Address
Rooms 3 to 5 from the north of Building 7, No. 28 Jinshan West Road, Yongkang Economic Development Zone, Jinhua City Zhejiang, China, 321300
Owner or operator
Zhejiang Jianrui Technology Co., Ltd (10091529)
Roles
Exporter to the US, Manufacturer
First device listed
October 12, 2024
Registered through
2026
Brand names listed
Electric 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
August 7, 2024K240255Electric Wheelchair (JLE-W01A-2023)ITISubstantially EquivalentZhejiang Jianrui Technology Company Limitedaccessdata.fda.gov

Compare with other makers

Updated August 7, 2024. 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.