Philips Respironics has issued another ventilator recall deemed the most serious type by the FDA as it may cause serious injury or death.

Airway Management proudly announces a historic milestone with the FDA clearance of Nylon flexTAP ® , the world’s first digitally printed single-point midline oral appliance device for sleep apnea.

Results from a multicenter clinical trial, now published in the European Journal of Pediatrics, represent a significant milestone in the fight against one of the most underdiagnosed and undertreated ...

Snoring and sleep apnea are issues that affect thousands of people across Hawai‘i, and while CPAP machines are often ...

Nyxoah announced today that it filed a lawsuit against Inspire Medical Systems alleging the infringement of sleep apnea ...

Philips Respironics has removed certain DreamStation devices due to programming errors that can result in failed therapy modes, according to the U.S. Food and Drug Administration.

Paris prosecutors opened a criminal probe into Philips in June over its recall of sleep apnea devices, probing possible ...

Here are four of the latest recalls and corrections reported to the FDA.

The research highlights an unsettling link between nighttime oxygen loss and long-term cognitive health. The team behind the ...

When people first hear about portable power stations, their immediate question is not about technical specifications but about real-world usefulness. Can this device keep my food cold during a ...

James Collins, a 29-year-old hospital administrator from Travis, couldn’t understand what was causing his chronic fatigue.

The fundamentals of the industry are driven by demographics, and broadening the scope provides a bit of growth opportunity,' ...