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Data / Medical devices / Abutment, Implant, Dental, Endosseous / China

FDA-registered makers of Abutment, Implant, Dental, Endosseous in China: 14 establishments

14 establishments in China are registered with the FDA to make Abutment, Implant, Dental, Endosseous (product code NHA). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Abutment, Implant, Dental, Endosseous
Product code
NHA
Country
China

Makers of Abutment, Implant, Dental, Endosseous in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
CBD Dental Lab, IncShenzhen Guangdong, ChinaManufacturer2October 17, 2023000api.fda.gov
Chengdu Besmile Medical Technology Co., Ltd.Chengdu Sichuan, ChinaManufacturer1September 2, 2025000api.fda.gov
Topway Dental Laboratory Co., LtdShenzhen Guangdong, ChinaManufacturer1October 20, 2004000api.fda.gov
Bio Concept Co., Ltd.Changzhou Jiangsu, ChinaManufacturer0000api.fda.gov
DTS Digital Dental Labshenzhen Guangdong, ChinaContract manufacturer0000api.fda.gov
Exceldent Dental Technology Development Co., Ltd.Zhuhai Guangdong, ChinaContract manufacturer0000api.fda.gov
Jiangsu Trausim Medical Instrument Co.,ltd.Changzhou Jiangsu, ChinaContract manufacturer, Manufacturer0000api.fda.gov
KTJ Medical Technology Co.,Ltd.Shenzhen Guangdong, ChinaContract manufacturer0000api.fda.gov
LX Precision Shanghai Co LtdShanghai, ChinaContract manufacturer0000api.fda.gov
Modern Dental Laboratory (DG) Co., Ltd.Dongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
New Perfect Dental LabSHENZHEN Guangdong, ChinaContract manufacturer0000api.fda.gov
Shimmer Computerized Dental Technology Co.,ltdZhuhai Guangdong, ChinaContract manufacturer0000api.fda.gov
Shenzhen Jiahong Dental Technology Co., LtdShenzhen Guangdong, ChinaContract manufacturer0000api.fda.gov
Zhuhai Crystal Dental Technology Co.,ltdZhuhai Guangdong, ChinaContract manufacturer, Contract sterilizer0000api.fda.gov

Updated November 3, 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.