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Data / Medical devices / Resin, Denture, Relining, Repairing, Rebasing / China

FDA-registered makers of Resin, Denture, Relining, Repairing, Rebasing in China: 12 establishments

12 establishments in China are registered with the FDA to make Resin, Denture, Relining, Repairing, Rebasing (product code EBI). 8 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
Resin, Denture, Relining, Repairing, Rebasing
Product code
EBI
Country
China

Makers of Resin, Denture, Relining, Repairing, Rebasing in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Yamahachi Dental Material (Changshu) Co., Ltd.Changshu city Jiangsu, ChinaManufacturer4March 5, 2024000api.fda.gov
Aidite (qinhuangdao) Technology Co., LtdQinhuangdao City Hebei, ChinaManufacturer3November 22, 2024000api.fda.gov
Shandong Huge Dental Material CorporationRizhao Shandong, ChinaManufacturer3May 6, 2026000api.fda.gov
Guangzhou Heygears Imc.incGuangzhou Guangdong, ChinaSpecification developer2August 13, 2026000api.fda.gov
Hangzhou Shining3d Dental Technology Co., LtdHangzhou Zhejiang, ChinaManufacturer1March 31, 2025000api.fda.gov
Ningbo Sezen Technology Co., Ltd.Ningbo Zhejiang, ChinaManufacturer1November 25, 2025000api.fda.gov
Riton 3D Technology Co., LtdGuangzhou Guangdong, ChinaManufacturer1December 23, 2024000api.fda.gov
Shen Fu Arts LabShen Zhen Guangdong, ChinaManufacturer1March 12, 1980000api.fda.gov
Huliang (shanghai) Bio-Tech Co., Ltd.Shanghai, ChinaManufacturer0000api.fda.gov
Jiangxi Heygears Innovative Material Co., LtdJiujiang Jiangxi, ChinaContract manufacturer0000api.fda.gov
Liaoning Upcera Co.,LtdBenxi Liaoning, ChinaManufacturer0000api.fda.gov
Shenzhen Piocreat 3D Technology Co., LtdShenzhen Guangdong, 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.