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Data / Medical devices / China / Guangdong Dayang Medical Technology Co.,ltd

Guangdong Dayang Medical Technology Co.,ltd: FDA-registered device maker in FOSHAN Guangdong, China, 1 510(k) clearance

Guangdong Dayang Medical Technology Co.,ltd is registered with the FDA (registration 3011781238) in FOSHAN Guangdong, China. It lists 9 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 21, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3011781238
Address
XINGXIAN DEVELOPMENT ZONE, CHANGHONGLING INDUSTRIAL PARK(2nd PHASE),SHISHAN,NANHAI DISTRICT, FOSHAN Guangdong, China, 528200
Owner or operator
GUANGDONG DAYANG MEDICAL TECHNOLOGY CO.,LTD (10083764)
Roles
Manufacturer
First device listed
December 17, 2021
Registered through
2026
Brand names listed
Bed Assist, CRUTCH, ELECTRIC TRANSFER CHAIR, MANUAL TRANSFER CHAIR, Manual Wheelchair (DY01903(2)), SHOWER CHAIR, COMMODE CHAIR, STICK, TRANSIT CHAIR and more

Devices it lists

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
May 21, 2026K254141Manual Wheelchair (DY01903(2))IORSubstantially EquivalentGuangdong Dayang Medical Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated May 21, 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.