Nyxoah NYXH recently received FDA approval for its Genio system, an innovative therapy for moderate to severe Obstructive Sleep Apnea (OSA). Featuring a leadless, battery-free design powered by an ...

The FDA has approved the Genio® system for treating patients with moderate to severe obstructive sleep apnea (OSA) with an ...

The FDA has approved the Genio system for the treatment of patients with moderate to severe obstructive sleep apnea.

After years of being cleared on the European market, Nyxoah’s neuromodulation therapy for obstructive sleep apnea has now ...

Nyxoah SA (NASDAQ:NYXH) saw its stock rise 9.4% after the FDA granted approval for its Genio system designed to treat ...

Genio is a different approach to hypoglossal nerve stimulation (HGNS) for the treatment of OSA. Genio’s unique design ...

Nyxoah announced today that it received FDA approval for its Genio neuromodulation device for treating sleep apnea.

NASHVILLE, Tenn. (Ivanhoe Newswire) - Obstructive sleep apnea is a medical condition that causes the upper airway to collapse during sleep. In fact, 40,000 people die from it each year.

NASHVILLE, Tenn. (Ivanhoe Newswire) – Obstructive sleep apnea is a medical condition that causes the upper airway to collapse during sleep – in fact, 40,000 die from it each year. Breathing ...

Nyxoah is in the midst of a lawsuit brought on by Inspire Medical Systems alleging infringement of several patents related to its recently-cleared offering, Genio.

NASHVILLE, Tn. - “Sleep apnea is also related to body weight. As body weight goes up, the throat gets increasingly collapsible at night, and it can become so collapsible that nothing else will ...

PRESS RELEASE GlobeNewswire Jan. 26, 2021, 01:02 AM PRESS RELEASE Nyxoah announces full-body 1.5T and 3T MRI compatibility for the Genio® system to treat Obstructive Sleep Apnea (OSA) ...