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Data / Medical devices / China / Zhuhai DS Dental Technology Co., Ltd

Zhuhai DS Dental Technology Co., Ltd: FDA-registered device maker in Zhuhai Guangdong, China, 1 510(k) clearance

Zhuhai DS Dental Technology Co., Ltd is registered with the FDA (registration 3013156109) in Zhuhai Guangdong, China. It lists 8 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 5, 2013. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3013156109
Address
3rd floor, Building F, Pingxi 10 road No. 6 Nanping Technology industrial park, Zhuhai Guangdong, China, 519000
Owner or operator
Zhuhai DS Dental Technology Co., LTD (10052660)
Roles
Manufacturer
First device listed
September 5, 2016
Registered through
2026
Brand names listed
Accessories, implant, dental, endosseous, BAR, PREFORMED, Dentures, full, Device, anti-snoring, Restoration, base metal, Restoration, noble metal, Restoration, porcelain, Restoration, porcelain-fused-to-metal

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
April 5, 2013K123410HEALTHY SLEEP APPLIANCELRKSubstantially EquivalentHealthy Sleep Dental Laboratoryaccessdata.fda.gov

Compare with other makers

Updated April 5, 2013. 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.