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United States Airway Management Industry Technologies | AI, Video Laryngoscopes & Smart Monitoring Shape Future Trends
Airway Management Industry
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Latest M&A Activity
In 2025, several medical device manufacturing companies expanded their airway management portfolios through acquisitions and strategic partnerships.
For example, Innovia Medical, backed by Inverness Graham, completed acquisitions of Grace Medical and Hurricane Medical, strengthening its position in single-use surgical instruments, including airway devices.
TEAM Technologies acquired medtech design firm TAG3 Engineering and cardiovascular delivery device company Duke Empirical, both expanding manufacturing and R&D capabilities relevant to airway and minimally invasive device platforms.
M&A activity is driven by demand for innovative, single-use, smarter airway devices that improve safety and efficiency in emergency and surgical care.
Key Players:
Medtronic , Boston Scientific Corporation , Olympus Corporation, ICU Medical, Inc, ConvaTec Group Plc, KARL STORZ, Teleflex Incorporated , Ambu A/S , Verathon Inc, SourceMark
Growth Forecast Projected:
The Global Airway Management Devices Market is anticipated to rise at a considerable rate during the forecast period, between 2025 and 2032. In 2024, the market is growing at a steady rate, and with the rising adoption of strategies by key players, the market is expected to rise over the projected horizon.
Research Process:
Both primary and secondary data sources have been used in the global Airway Management Devices Market research report. During the research process, a wide range of industry-affecting factors are examined, including governmental regulations, market conditions, competitive levels, historical data, market situation, technological advancements, upcoming developments, in related businesses, as well as market volatility, prospects, potential barriers, and challenges.
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Key Segments:
By Type: (Laryngoscopes, Infraglottic Airway Management Devices, Supraglottic Airway Management Devices, Resuscitators, Cricothyrotomy Kits, Others)
By Age: (Pediatrics/Neonates, Adults)
By End User: (Hospitals, Ambulatory Surgical Centers, Others)
Regional Analysis for Market:
⇥ North America (U.S., Canada, Mexico)
⇥ Europe (U.K., Italy, Germany, Russia, France, Spain, The Netherlands and Rest of Europe)
⇥ Asia-Pacific (India, Japan, China, South Korea, Australia, Indonesia Rest of Asia Pacific)
⇥ South America (Colombia, Brazil, Argentina, Rest of South America)
⇥ Middle East & Africa (Saudi Arabia, U.A.E., South Africa, Rest of Middle East & Africa)
Regulatory Approvals and FDA Clearances (2025)
The global airway management devices market is projected to grow from approximately USD 1.78 billion in 2025 to USD 2.49 billion by 2035, at a CAGR of 3.4%, driven by heightened respiratory disease incidence and surgical needs.
FDA clearances received by several novel devices in 2025 include:
Synchrony Medical's LibAirty Airway Clearance System (510(k) clearance) for home-use airway clearance in chronic lung disease patients.
Airway Management's Nylon flexTAP® custom oral appliance for obstructive sleep apnea received FDA clearance as a digitally 3D printed patient-specific device.
Regulatory emphasis is on compliance with ISO standards (ISO 5361 & ISO 5356-1) for safety, sterility, and functionality testing of airway tubes and devices.
Vitaltec Corporation's Rota-Trach Tracheostomy Tubes received CDSCO (India) approval in 2025, marking expanded regulatory acceptance in emerging markets.
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Latest Market News & Trends
The airway management device market is increasingly focusing on single-use, biocompatible, and sensor-integrated products to reduce infection risks and improve patient outcomes in hospitals and homecare.
Technologies like 3D printing and digitally customized appliances for sleep apnea and airway obstruction are becoming mainstream, enabling precise fit, comfort, and compliance.
Growing chronic respiratory conditions worldwide, plus rising surgical procedures needing airway support, are boosting market growth combined with heightened regulatory scrutiny
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