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Data / Medical devices / Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Sterile / China

FDA-registered makers of Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Sterile in China: 10 establishments

10 establishments in China are registered with the FDA to make Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Sterile (product code MCF). 0 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
Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Sterile
Product code
MCF
Country
China

Makers of Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Sterile in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Cixi Seago Electronics Co.,ltdNINGBO Zhejiang, ChinaManufacturer0000api.fda.gov
Guangdong Souncrise Technology Co.,ltdZhuhai Guangdong, ChinaManufacturer0000api.fda.gov
Hangzhou Yunchi Technology Co., LtdHangzhou Zhejiang, ChinaContract manufacturer, Exporter to the US, Manufacturer, Remanufacturer0000api.fda.gov
Hefei MT Medical Co.,ltd.Hefei Anhui, ChinaExporter to the US, Manufacturer0000api.fda.gov
Ningbo Seago Electric Co.,ltdNingbo Zhejiang, ChinaManufacturer0000api.fda.gov
Qibei Technology Co., LimitedKL Hong Kong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Shenzhen Besman Electronic Technology Co., LtdShenzhen Guangdong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Shenzhen Relish Technology Co.,ltdShenzhen Guangdong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Shenzhen Fortunecome Technology Co.,Ltd.Shenzhen Guangdong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Yangzhou Super J Toothbrush Co.,ltd.Guangling District Jiangsu, ChinaExporter 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.