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Data / Medical devices / Mattress, Air Flotation, Alternating Pressure / Taiwan

FDA-registered makers of Mattress, Air Flotation, Alternating Pressure in Taiwan: 13 establishments

13 establishments in Taiwan are registered with the FDA to make Mattress, Air Flotation, Alternating Pressure (product code FNM). 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
Mattress, Air Flotation, Alternating Pressure
Product code
FNM
Country
Taiwan

Makers of Mattress, Air Flotation, Alternating Pressure in Taiwan

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Air Kinetic Technologies Corp.Pingzhen Dist. Taoyuan, TaiwanManufacturer0000api.fda.gov
BenQ Medical Technology CorporationTaoyuan City, TaiwanContract manufacturer0000api.fda.gov
Caremed Supply, Inc.New Taipei City, TaiwanContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Caremed Supply, Inc.Yilan County, TaiwanContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Cathay Consolidated Inc.Yilan, TaiwanContract manufacturer0000api.fda.gov
Care&Care Health Products Co., LtdYuanli Township Miaoli, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Carilex Medical, Inc.Guishan District Taoyuan, TaiwanManufacturer0000api.fda.gov
Eezcare Medical Corp.Tucheng Dist, New Taipei City, TaiwanManufacturer0000api.fda.gov
Jochu Technology Co., LtdHsin Chu Hsinchu(County), TaiwanManufacturer0000api.fda.gov
Rong Shin Industrial Co., Ltd.Tainan City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Sequoia-Twn Healthcare Co. Ltd.New Taipei City, TaiwanManufacturer0000api.fda.gov
Valentine Intl. Ltd.Hsichih City, Taipei Hsien, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Wellell Inc.New Taipei City, TaiwanContract manufacturer, 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.