The FDA has granted clearance for a new prescription device, the iNOS intraoral biosensor, designed to treat sleep apnea and reduce snoring. This development is significant because it integrates continuous blood oxygen monitoring directly into an oral appliance, allowing for more precise assessment of therapy effectiveness and potentially improving patient outcomes related to sleep-disordered breathing. A soft launch is planned for October, with broader availability expected in early 2027.
Read the full article at Sleep Review
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