Airolign
A Smarter Balloon for Nasal Airway Realignment
Our Solution: Airolign
Airolign is a proprietary balloon-based device engineered to perform safe, consistent, and effective balloon septo-turbinatoplasty.
Using controlled insufflation pressure, Airolign gently realigns the nasal septum and laterally displaces (out-fractures) the inferior turbinates creating more space in the nasal airway.
Unlike prior ENT balloons, Airolign is optimized specifically for the septum and turbinate anatomy.
Its novel shape, pressure-regulated inflation system, and ease-of-use design enable ENT physicians to deliver a reproducible outcome with minimal patient discomfort.
What Makes Airolign Different
How It Works
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Preparation
Local anesthesia is administered. The Airolign balloon is gently inserted into the nasal passage, aligning with the septum or turbinate area.
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Controlled Inflation
The balloon is inflated to a pre-set pressure using the Airolign insufflation system, gently shifting and realigning the bony and cartilaginous structures.
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Realigned Structure
The structures are gently repositioned, temporarily opening the airway by controlled balloon expansion.
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Controlled Removal
The device is deflated and removed. No tissue is cut, no sutures required, and patients experience minimal downtime.
Indications for Use
Airolign is intended for patients suffering from:
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Nasal airway obstruction due to septal deviation
Blocked airflow caused by a deviated septum.
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Candidates for non-invasive or in-office treatment
Suitable for patients seeking quick, minimally invasive solutions.
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Compensatory turbinate hypertrophy
Enlarged turbinates contributing to nasal blockage.
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Chronic nasal congestion unresponsive to medical management
Persistent symptoms despite medication.
Benefits at a glance
No general anesthesia
Our approach eliminates the need for general anesthesia, making the procedure safer and easier for patients.
What’s Next
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01
Concept & Prototype Development
Initial design and prototyping of Airolign’s patented trapezoidal balloon — engineered for safe, controlled septal realignment.
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02
Preclinical Validation
Cadaveric and bench testing confirm precise septal correction, turbinate out-fracture, and consistent usability across cases.
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03
Regulatory Alignment
FDA pre-submission completed with 510(k) pathway confirmed — streamlining the route to market approval.
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04
Clinical Evaluation & Market Entry
Formative usability testing and early physician adoption begin, supported by training, data collection, and distributor partnerships.
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05
Next-Gen AI Integration
Future phase introduces AI-guided pressure control and CT-based optimization — advancing Airolign from device to intelligent platform.
What Clinicians
& Advisors Are Saying
Trusted voices in ENT and MedTech are already recognizing the impact Airolign could have on nasal airway treatment. Here's what they’re saying:
Sign Up for Early Access
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