Skip to the page

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

Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Sterile (MCF): 14 FDA-registered makers in 4 countries

14 establishments in 4 countries are registered with the FDA to make Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Sterile (product code MCF, Class 1, 21 CFR 872.6855). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 5 510(k) clearances under this code, the latest on May 28, 2003, and lists 1 recall event (0 Class I). 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.

Product code
MCF
Device class
1
Regulation
872.6855
Medical specialty
Dental

Makers by country

CountryMakers
China10
South Korea2
United States1
Thailand1

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

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Ashtel Studios, Inc.Ontario, CA, United StatesSpecification developer0000api.fda.gov
BTB Korea Co.,LtdSeongnam Gyeonggi, South KoreaManufacturer0000api.fda.gov
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
Seago Electronics(thailand)co.,ltdSriracha Chon Buri, ThailandManufacturer0000api.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
Uzinmedicare Co., Ltd.Hwaseong-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
Yangzhou Super J Toothbrush Co.,ltd.Guangling District Jiangsu, ChinaExporter to the US, Manufacturer0000api.fda.gov

Updated May 28, 2003. 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.