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Data / Medical devices / Stimulator, Nerve, Transcutaneous, For Pain Relief / Taiwan

FDA-registered makers of Stimulator, Nerve, Transcutaneous, For Pain Relief in Taiwan: 11 establishments

11 establishments in Taiwan are registered with the FDA to make Stimulator, Nerve, Transcutaneous, For Pain Relief (product code GZJ). 9 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
Stimulator, Nerve, Transcutaneous, For Pain Relief
Product code
GZJ
Country
Taiwan

Makers of Stimulator, Nerve, Transcutaneous, For Pain Relief in Taiwan

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Well-Life Healthcare LimitedJhonghe Taipei, TaiwanManufacturer6January 17, 2017000api.fda.gov
Gemore Technology Co., Ltd.TAN SHUI New Taipei, TaiwanManufacturer5December 21, 2012000api.fda.gov
Everyway Medical Instruments Co., Ltd.New Taipei City, TaiwanManufacturer3September 5, 2007000api.fda.gov
Zmi Electronics Ltd.Kaohsiung, TaiwanContract manufacturer, Manufacturer2July 18, 1983000api.fda.gov
Besmed Health Business CorporationNew Taipei City, TaiwanExporter to the US, Manufacturer1November 28, 2003000api.fda.gov
Coforce Medical Co., Ltd.New Taipei City, TaiwanSpecification developer1August 26, 2022000api.fda.gov
Everlife Medical Equipment Co., Ltd.New Taipei City, TaiwanContract manufacturer, Manufacturer1November 27, 2007000api.fda.gov
Ten Comfort Corp.New Taipei City, TaiwanExporter to the US, Manufacturer1January 27, 1994000api.fda.gov
Valentine Intl. Ltd.Hsichih City, Taipei Hsien, TaiwanExporter to the US, Manufacturer1December 10, 2003000api.fda.gov
Astek Technology Ltd.Tainan, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Domex Technology CorporationHsinchu Hsinchu(County), TaiwanContract 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.