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Data / Medical devices / Denture Preformed (Partially Prefabricated Denture) / China

FDA-registered makers of Denture Preformed (Partially Prefabricated Denture) in China: 7 establishments

7 establishments in China are registered with the FDA to make Denture Preformed (Partially Prefabricated Denture) (product code EKO). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Denture Preformed (Partially Prefabricated Denture)
Product code
EKO
Country
China

Makers of Denture Preformed (Partially Prefabricated Denture) in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Xiao Fei Dental Manufacture (Chengdu) Co.LtdCHENGDU Sichuan, ChinaManufacturer1October 15, 1976000api.fda.gov
Foo Tian Dental LaboratoryShenzhen Guangdong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Guangzhou Jinguanqiao Industry Co., LtdGuangzhou Guangdong, ChinaManufacturer0000api.fda.gov
Nanjing Chamlion Laser Technology Co., Ltd.Nanjing Jiangsu, ChinaExporter to the US, Manufacturer0000api.fda.gov
Qinhuangdao Audental Metal Technology Co., Ltd.Qinhuangdao City Hebei, ChinaManufacturer0000api.fda.gov
Shenzhen Jiahong Dental Technology Co., LtdShenzhen Guangdong, ChinaContract manufacturer0000api.fda.gov
Xi'an Sinotitanium Metals Co.,ltdXi an Shaanxi, ChinaManufacturer0000api.fda.gov

Updated November 2, 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.