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Data / Medical devices / Orthosis, Corrective Shoe / Taiwan

FDA-registered makers of Orthosis, Corrective Shoe in Taiwan: 14 establishments

14 establishments in Taiwan are registered with the FDA to make Orthosis, Corrective Shoe (product code KNP). 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
Orthosis, Corrective Shoe
Product code
KNP
Country
Taiwan

Makers of Orthosis, Corrective Shoe in Taiwan

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Comfort Plus CorporationNew Taipei City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Da Yu Enterprise Co., Ltd.Tianzhong Township Changhua, TaiwanContract manufacturer, Manufacturer0000api.fda.gov
E-Life International Co., LtdYonghe Dist., Taipei, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Fung Lead Medical & Sports Co., Ltd.Nantou City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Fung Yin Industrial Co LtdNantou, TaiwanManufacturer0000api.fda.gov
Homeway Technology Co. Ltd.Tainan, 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
Maxhealth Corp.Xizhi District, New Taipei City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
More Medical Global Co., LtdTaichung City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Top Longmax Products Co., Ltd.Taichung, TaiwanContract manufacturer0000api.fda.gov
Top Medical Corp.Chung Li City Taoyuan, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Yong Tai Global Co., Ltd.Tainan City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Yuea Tay Industrial Co LtdTaichung City, TaiwanManufacturer0000api.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.