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Data / Medical devices / Insoles, Medical / Taiwan

FDA-registered makers of Insoles, Medical in Taiwan: 14 establishments

14 establishments in Taiwan are registered with the FDA to make Insoles, Medical (product code KYS). 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
Insoles, Medical
Product code
KYS
Country
Taiwan

Makers of Insoles, Medical in Taiwan

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Comfort Plus CorporationNew Taipei City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Fusco Tek LLCShengang District, Taichung City, TaiwanManufacturer0000api.fda.gov
Horsing Enterprises Co LtdTaichung, TaiwanContract manufacturer, Manufacturer0000api.fda.gov
I-Ming Sanitary Materials Co., Ltd.Changhua, TaiwanManufacturer0000api.fda.gov
Jiundar Industrial Co., Ltd.SHULIN CITY Taipei, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Mammon International Corp.Taipei City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Overland Int'l CorporationNew Taipei City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Paifu Comfort Industrial Co LtdTainan City, TaiwanContract manufacturer, Manufacturer0000api.fda.gov
Power Well Healthcare Technology Co., Ltd.Changhua County, TaiwanExporter to the US, Manufacturer0000api.fda.gov
R&R Medical Corporation Ltd.Sanchong District New Taipei, TaiwanManufacturer0000api.fda.gov
Special Protectors Co., Ltd.New Taipei City, TaiwanManufacturer0000api.fda.gov
Tien Jiang Enterprise Co., Ltd.Tainan City, TaiwanContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Top Longmax Products Co., Ltd.Taichung, TaiwanContract manufacturer0000api.fda.gov
Valentine Intl. Ltd.Hsichih City, Taipei Hsien, TaiwanExporter to the US, Manufacturer0000api.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.