FDA grants 510(k) clearance to snoring-reducing device

The FDA has granted 510(k) clearance to Mouth Guard+, a mandibular advancement device designed to reduce snoring, according to a press release from SnoreLessNow.
“This clearance will give clinicians an opportunity to recommend an alternative snoring solution to patients who are noncompliant or uncomfortable with CPAP use,” Chris Garvey, BS, chief operating officer and co-founder of SnoreLessNow, told Healio.
According to Garvey, the Mouth Guard+ dental appliance allows an individual to get maximum airflow while sleeping by gently nudging their jaw forward.
One key feature of the

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