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Data / Medical devices / Locator, Root Apex / China

FDA-registered makers of Locator, Root Apex in China: 8 establishments

8 establishments in China are registered with the FDA to make Locator, Root Apex (product code LQY). 6 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
Locator, Root Apex
Product code
LQY
Country
China

Makers of Locator, Root Apex in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Changzhou Bomedent Medical Technology Co., LtdChangzhou Jiangsu, ChinaManufacturer1March 30, 2021000api.fda.gov
Changzhou Sifary Medical Technology Co., Ltd.Changzhou Jiangsu, ChinaManufacturer1April 8, 2026000api.fda.gov
Foshan Coxo Medical Instrument Co., Ltd.Foshan Guangdong, ChinaManufacturer1July 20, 2022000api.fda.gov
Guilin Woodpecker Medical Instrument Co., LtdGUILIN CITY Guangxi, ChinaManufacturer1December 18, 2018000api.fda.gov
Shenzhen Rogin Medical Co., Ltdshenzhen Guangdong, ChinaExporter to the US, Manufacturer1March 7, 2025000api.fda.gov
Shenzhen Superline Technology Co.,ltdShenzhen Guangdong, ChinaManufacturer1January 17, 2025000api.fda.gov
Denjoy Dental Co., LtdChangsha city Hunan, ChinaManufacturer0000api.fda.gov
Shenzhen Perfect Medical Instruments Co., Ltd.Shenzhen 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.