ResMed
Publicly traded manufacturer of sleep apnea and connected respiratory care devices.
Updated Jul 1, 2026
Headquartered in San Diego, California, United States
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Overview
About ResMed
ResMed is headquartered in San Diego, California, and publicly traded on the NYSE. Originally founded in Australia, the company manufactures CPAP and sleep apnea therapy devices, ventilators, and connected digital health software for respiratory care used in more than 140 countries.
Products
- CPAP & sleep apnea therapy devices
- Ventilators
- Connected respiratory care software (myAir, AirView)
Markets Served
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Related
Certifications
ISO 13485
The international quality management system standard specific to medical device manufacturers, referenced by most major regulators.
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CE Mark
The conformity mark required to sell medical devices in the EU/EEA, issued once a device meets EU MDR or IVDR requirements.
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FDA 510(k) / PMA
US market authorization for medical devices via the FDA's 510(k), De Novo, or PMA pathways.
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EU MDR
The EU regulation that defines medical device requirements — CE Marking is the certification mark it produces once satisfied.
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Related
Regulatory Pathways
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