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Data / Medical devices / Cannula, Nasal, Oxygen / Taiwan

FDA-registered makers of Cannula, Nasal, Oxygen in Taiwan: 16 establishments

16 establishments in Taiwan are registered with the FDA to make Cannula, Nasal, Oxygen (product code CAT). 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
Cannula, Nasal, Oxygen
Product code
CAT
Country
Taiwan

Makers of Cannula, Nasal, Oxygen in Taiwan

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Besmed Health Business CorporationNew Taipei City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Create Biotech Co., Ltd.Taoyuan City, TaiwanManufacturer0000api.fda.gov
Enter Medical CorporationChiayi County Chiayi(County), TaiwanExporter to the US, Manufacturer0000api.fda.gov
Foremount Enterprise Co., Ltd.Taichung City, TaiwanContract manufacturer, Manufacturer0000api.fda.gov
Fortune Medical Instrument Corp.Taoyuan City, TaiwanContract manufacturer0000api.fda.gov
Foxxmed LtdIlan Yilan, TaiwanManufacturer0000api.fda.gov
Galemed Corp.WU-JIA Yilan, TaiwanContract manufacturer, Manufacturer0000api.fda.gov
Great Group Medical Co Ltd.Changhua County, TaiwanContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Headstar Medical Products Co., LtdNew Taipei City, TaiwanManufacturer0000api.fda.gov
Hsiner Co., Ltd.Taichung City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Hsiner Co., Ltd.Taichung City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Non-Change Enterprise Co., Ltd.New Taipei City, TaiwanContract manufacturer, Manufacturer0000api.fda.gov
Omnimate Enterprise Co., Ltd.Ilan County Yilan, TaiwanContract manufacturer, Manufacturer0000api.fda.gov
Sunder Biomedical Tech. Co., Ltd.Yunlin County, TaiwanManufacturer0000api.fda.gov
VADI Medical Technology Co., Ltd.Taoyuan City, TaiwanManufacturer0000api.fda.gov
Valentine Intl. Ltd.Hsichih City, Taipei Hsien, TaiwanExporter to the US, 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.