Global Partner
×

Nylon flexTAP® Becomes the First FDA cleared 3D-Printed Midline Oral Appliance for Sleep Apnea 

Nylon flexTAP® Becomes the First FDA cleared 3D-Printed Midline Oral Appliance for Sleep Apnea 
News, Products
DALLAS, TX (September 17, 2025) – 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. Launched today, this revolutionary device redefines patient care by combining cutting-edge patented Vertex Technology® with unparalleled comfort and efficacy, now FDA cleared for mild to moderate obstructive sleep apnea (OSA).

Key Features and Benefits

  “We are thrilled to introduce the Nylon flexTAP, a game-changer in oral appliance therapy,” said Charles Collins, CEO of Airway Management. “Feedback from key opinion leaders in our TAP Sleep Care system highlights its superior effectiveness and patient comfort. Peer-reviewed studies also confirm that our patented mouth shield, which promotes nasal breathing, significantly improves treatment outcomes. This innovation underscores our commitment to advancing sleep health.”

A New Standard in Sleep Apnea Treatment

Since 2015, the American Academy of Sleep Medicine (AASM) and American Academy of Dental Sleep Medicine (AADSM) have recommended oral appliance therapy for mild to moderate sleep apnea. The Nylon flexTAP sets a new benchmark by leveraging digital printing technology to create the first FDA-approved single-point midline device, eliminating the need for bite registration while maintaining precision.  Manufactured in the U.S.A., the device is now available through Airway Labs, with PDAC coverage (E0486) pending.

Get Started Today

Ready to send a case? Order now through Airway Labs.
Airway Labs logo

Airway Labs is the leading production facility of the TAP oral appliances for snoring and obstructive sleep apnea.