Please provide your email address to receive an email when new articles are posted on . Positive airway pressure device compliance decreased between 30 days after a clinic visit and 90 days.

Please provide your email address to receive an email when new articles are posted on . Air pollution concentrations, even at relatively low levels, were associated with a change in the effectiveness ...

SAN DIEGO, Feb. 12, 2024 (GLOBE NEWSWIRE) -- ResMed (NYSE: RMD, ASX: RMD) launched today its AirCurve 11 series devices, the company’s newest bilevel devices that use two levels of support, ...

Lawmakers requested the report after a 2023 ProPublica and Pittsburgh Post-Gazette investigation revealed that the FDA had ...

More than a year after the start of a recall now involving more than 5 million breathing devices, doctors and patients are still feeling the effects as manufacturer Philips continues to remediate ...

CAMBRIDGE, Mass.--(BUSINESS WIRE)--Apnimed, a clinical-stage pharmaceutical company focused on developing oral pharmacologic therapies for the treatment of obstructive sleep apnea (OSA) and related ...

Medical device company ResMed has received U.S. Food and Drug Administration (FDA) 510 (k) clearance for its AirMini portable continuous positive airway pressure (CPAP) device. The AirMini is a small, ...

LINCOLN, Neb. (KOLN) - Sleep apnea, a disorder that causes repeated pauses in breathing throughout the night, currently affects about 25 million Americans. But at CHI Health St. Elizabeth, one man ...

There is currently no drug that treats sleep apnea. However, the third clinical trial of AD109 suggests there could be one in the future. Taylor Leamey wrote about all things wellness for CNET, ...

The failure to quickly and clearly communicate information about recall notices to patients with home-use medical devices is the top health technology hazard of 2023, according to nonprofit safety ...