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Data / Medical devices / Implant, Endosseous, Root-Form / China

FDA-registered makers of Implant, Endosseous, Root-Form in China: 7 establishments

7 establishments in China are registered with the FDA to make Implant, Endosseous, Root-Form (product code DZE). 3 have 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
Implant, Endosseous, Root-Form
Product code
DZE
Country
China

Makers of Implant, Endosseous, Root-Form in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Bio Concept Co., Ltd.Changzhou Jiangsu, ChinaManufacturer3August 10, 2022000api.fda.gov
Chengdu Besmile Medical Technology Co., Ltd.Chengdu Sichuan, ChinaManufacturer1February 2, 2026000api.fda.gov
Jiangsu Trausim Medical Instrument Co.,ltd.Changzhou Jiangsu, ChinaContract manufacturer, Manufacturer1December 12, 2014000api.fda.gov
Basic (chengdu) Medical Device Co., Ltd.chengdu Sichuan, ChinaContract manufacturer0000api.fda.gov
Changzhou Biomet Medical Devices Co., Ltd.Changzhou City Jiangsu, ChinaContract manufacturer0000api.fda.gov
Dongguan Xinlonghong Hardware Co., LtdDongguan City Guangdong, ChinaContract manufacturer0000api.fda.gov
LX Precision Shanghai Co LtdShanghai, ChinaContract manufacturer0000api.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.