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Data / Medical devices / Monitor, Airway Pressure (Includes Gauge And/Or Alarm) / China

FDA-registered makers of Monitor, Airway Pressure (Includes Gauge And/Or Alarm) in China: 7 establishments

7 establishments in China are registered with the FDA to make Monitor, Airway Pressure (Includes Gauge And/Or Alarm) (product code CAP). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Monitor, Airway Pressure (Includes Gauge And/Or Alarm)
Product code
CAP
Country
China

Makers of Monitor, Airway Pressure (Includes Gauge And/Or Alarm) in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
GaleMed (Xiamen) Co., Ltd.XIAMEN Fujian, ChinaManufacturer1November 18, 2010000api.fda.gov
AMBU LimitedXIANG YU F.T.Z., XIAMEN Fujian, ChinaContract manufacturer0000api.fda.gov
Amphenol Medical Technologies (Dongguan) Co., Ltd.Dongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Flexicare Medical (dongguan) Ltd.DONGGUAN CITY Guangdong, ChinaContract manufacturer0000api.fda.gov
Ge Medical Systems (china) Co., Ltd.WUXI Jiangsu, ChinaSpecification developer0000api.fda.gov
Laerdal Medical (suzhou) Co., Ltd.215009 Suzhou Jiangsu Province, ChinaManufacturer0000api.fda.gov
Vincent Medical (dong Guan) Manufacturing Co., Ltd.Dong Guan City Guangdong, ChinaContract 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.