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Data / Medical devices / China / Hebei Dansong Medical Technology Co., Ltd.

Hebei Dansong Medical Technology Co., Ltd.: FDA-registered device maker in SHIJIAZHUANG Hebei, China, 1 510(k) clearance

Hebei Dansong Medical Technology Co., Ltd. is registered with the FDA (registration 3043165991) in SHIJIAZHUANG Hebei, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 3, 2025. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3043165991
Address
#1 Office Building, Donghua Guoyuefu, Yuhua District, SHIJIAZHUANG Hebei, China, 050031
Owner or operator
HEBEI DANSONG MEDICAL TECHNOLOGY CO., LTD. (10094898)
Roles
Manufacturer
First device listed
January 4, 2026
Registered through
2026
Brand names listed
Electric Wheelchair (NSDS-01)

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
November 3, 2025K252671Electric wheelchair (NSDS-01)ITISubstantially EquivalentHebei Dansong Medical Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated November 3, 2025. 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.