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Data / Medical devices / China / Guangdong Yadeng Medical Apparatus Co.,ltd

Guangdong Yadeng Medical Apparatus Co.,ltd: FDA-registered device maker in Foshan Guangdong, China, 1 510(k) clearance

Guangdong Yadeng Medical Apparatus Co.,ltd is registered with the FDA (registration 3043582432) in Foshan Guangdong, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 27, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3043582432
Address
Factory 2, No.12, Fenggong Road, Nansha Industrial Zone, Danzao Town, Nanhai District, Foshan Guangdong, China, 528216
Owner or operator
Guangdong Yadeng Medical Apparatus Co.,Ltd (10095380)
Roles
Manufacturer
First device listed
March 5, 2026
Registered through
2026
Brand names listed
Integral Dental Unit Model: YD-A4, AD-S1, AD-S3, AD-S6

Devices it lists

DeviceProduct codeClassRoleSource
Chair, Dental, With Operative UnitKLC1Manufactureraccessdata.fda.gov
Unit, Operative DentalEIA1Manufactureraccessdata.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
June 27, 2025K243130Integral Dental UnitEIASubstantially EquivalentGuangdong Yadeng Medical Apparatus Co., Ltd.,accessdata.fda.gov

Compare with other makers

Updated June 27, 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.