Airway Management Receives FDA Clearance for Digitally Printed Sleep Apnea Device
U.S.-based medical device company Airway Management has received FDA clearance for the Nylon flexTAP, described as the world’s first digitally printed single-point midline oral appliance for sleep apnea. The device, manufactured in the U.S., combines the company’s patented Vertex Technology with a design intended for patients with mild to moderate obstructive sleep apnea (OSA). By using digital printing, the Nylon flexTAP enables a custom fit without requiring bite registration, which can simplify the fitting process for clinicians and patients.