Skip to the page

Data / Medical devices / Preparer, Root Canal Endodontic / China

FDA-registered makers of Preparer, Root Canal Endodontic in China: 8 establishments

8 establishments in China are registered with the FDA to make Preparer, Root Canal Endodontic (product code EKQ). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Preparer, Root Canal Endodontic
Product code
EKQ
Country
China

Makers of Preparer, Root Canal Endodontic in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Beijing C-Root Dental Medical Devices Co., Ltd.Beijing, ChinaManufacturer0000api.fda.gov
Changzhou Bomedent Medical Technology Co., LtdChangzhou Jiangsu, ChinaManufacturer0000api.fda.gov
Foshan Oreck Medical Technology Co.,ltdFoshan City Guangdong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Guilin Kevin Peter Technology Co., Ltd.Guilin Guangxi, ChinaManufacturer0000api.fda.gov
GUILIN YIKESHI Medical Device CO LTDGuilin Guangxi, ChinaManufacturer0000api.fda.gov
Hantech Medical Device Co., Ltd.Cixi Zhejiang, ChinaContract manufacturer0000api.fda.gov
Huizhou Videya Technology Co., Ltd.Huizhou Guangdong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Shandong Hengfeng Kerui Medical Equipment Co., LtdQingdao City Shandong, ChinaContract manufacturer, Exporter to the US, 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.