Skip to the page

Data / Medical devices / China / Golden Motor Technology Co., Ltd

Golden Motor Technology Co., Ltd: FDA-registered device maker in Changzhou Jiangsu, China, 1 510(k) clearance

Golden Motor Technology Co., Ltd is registered with the FDA (registration 3021959198) in Changzhou Jiangsu, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 21, 2022. 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
3021959198
Address
Room 1401-1405, No. 18-50 Middle Changwu Road, Changzhou Jiangsu, China, 213164
Owner or operator
Golden Motor Technology Co., Ltd (10084306)
Roles
Manufacturer
First device listed
February 8, 2022
Registered through
2026
Brand names listed
e-Throne Folding Wheelchairs

Devices it lists

DeviceProduct codeClassRoleSource
Wheelchair, PoweredITI2Manufactureraccessdata.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
January 21, 2022K191105e-Throne Folding Wheelchair, Model: ET-12F22ITISubstantially EquivalentGolden Motor Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated January 21, 2022. 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.