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Data / Medical devices / Condenser, Heat And Moisture (Artificial Nose) / Taiwan

FDA-registered makers of Condenser, Heat And Moisture (Artificial Nose) in Taiwan: 12 establishments

12 establishments in Taiwan are registered with the FDA to make Condenser, Heat And Moisture (Artificial Nose) (product code BYD). 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
Condenser, Heat And Moisture (Artificial Nose)
Product code
BYD
Country
Taiwan

Makers of Condenser, Heat And Moisture (Artificial Nose) 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
Foremount Enterprise Co., Ltd.Taichung City, TaiwanContract manufacturer, Manufacturer, Repackager or relabeler0000api.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
Hsiner Co., Ltd.Taichung City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Hsiner Co., Ltd.Taichung City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Kung Shin Plastics Co., Ltd.New Taipei City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Non-Change Enterprise Co., Ltd.New Taipei City, TaiwanContract manufacturer, Manufacturer0000api.fda.gov
Saykia CorporationChanghua County, TaiwanManufacturer0000api.fda.gov
VADI Medical Technology Co., Ltd.Taoyuan City, TaiwanManufacturer0000api.fda.gov
Yasco Enterprise Corp.Chiayi County Chiayi(County), 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.