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Data / Medical devices / Massager, Therapeutic, Electric / Taiwan

FDA-registered makers of Massager, Therapeutic, Electric in Taiwan: 16 establishments

16 establishments in Taiwan are registered with the FDA to make Massager, Therapeutic, Electric (product code ISA). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Massager, Therapeutic, Electric
Product code
ISA
Country
Taiwan

Makers of Massager, Therapeutic, Electric in Taiwan

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Astek Technology Ltd.Tainan, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Biboting International Co., LtdTaoyuan City, TaiwanManufacturer0000api.fda.gov
Besmed Health Business CorporationNew Taipei City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Fourstar Group Inc.Taipei, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Gemore Technology Co., Ltd.TAN SHUI New Taipei, TaiwanManufacturer0000api.fda.gov
Hivox Biotek Inc.New Taipei City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Home Care Technology Co., Ltd.Tainan City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Inno-Health Technology Co., Ltd.Taichung City, TaiwanManufacturer0000api.fda.gov
King Ultrasonic Co., Ltd.New Taipei City, TaiwanManufacturer0000api.fda.gov
Norte Sirius Enterprise Co., Ltd.CHUNG-HO CITY Taipei, TaiwanManufacturer0000api.fda.gov
Sun-Shine Land Intl. Ltd.Tamsui Taipei, TaiwanManufacturer0000api.fda.gov
Sunjoy Enterprises LimitedNew Taipei City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Ta Lai Sporting Goods Enterprises Co. Ltd.New Taipei City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Ten Comfort Corp.New Taipei City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Valentine Intl. Ltd.Hsichih City, Taipei Hsien, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Yankang Medical Instrument Co., Ltd.Taipei, TaiwanContract manufacturer, Manufacturer, Specification developer0000api.fda.gov

Updated November 3, 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.