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Data / Medical devices / Components, Wheelchair / Taiwan

FDA-registered makers of Components, Wheelchair in Taiwan: 15 establishments

15 establishments in Taiwan are registered with the FDA to make Components, Wheelchair (product code KNN). 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
Components, Wheelchair
Product code
KNN
Country
Taiwan

Makers of Components, Wheelchair in Taiwan

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Chang Cheng Fa Enterprise Co., LimitedSHI-KOOU SHIANG Chiayi(County), TaiwanManufacturer0000api.fda.gov
Care&Care Health Products Co., LtdYuanli Township Miaoli, TaiwanExporter to the US, Manufacturer0000api.fda.gov
D & C Products Corp.Taipei, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Freerider, Corp.Kaohsiung, TaiwanManufacturer0000api.fda.gov
Genemax Medical Products Industry Corp.Taichung City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Heartway Medical Products Co., Ltd.Taichung City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Hong Ming Enterprise Co., Ltd.Taichung City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Majesty-Tech Product Development Corp.Taipei City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Merits Health Products Co., Ltd.Taichung City, TaiwanManufacturer0000api.fda.gov
Optimal Medical Co., Ltd.Taichung City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Pihsiang Machinery MFG. Co., Ltd.HSINCHU COUNTY Hsinchu(County), TaiwanManufacturer0000api.fda.gov
Taiwan King Strong Co., Ltd.Taichung City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Valentine Intl. Ltd.Hsichih City, Taipei Hsien, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Wu Ho Medical Instruments MFG. Co. Ltd.Taipei Hsien, Taiwan, (China), TaiwanManufacturer0000api.fda.gov
Wu's Tech Co., Ltd.Hsin-Chu City Hsinchu(County), 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.