Airway Clearance System Market by Device Type (High Frequency Chest Wall Oscillation Device, Manual Chest Physiotherapy, Mechanical Vibrator), Indication (Bronchiectasis, Chronic Obstructive Pulmonary Disease, Cystic Fibrosis), End User, Distribution Chan
Description
The Airway Clearance System Market was valued at USD 703.39 million in 2024 and is projected to grow to USD 735.23 million in 2025, with a CAGR of 6.05%, reaching USD 1,125.41 million by 2032.
A concise and authoritative introduction framing the clinical importance, technology evolution, and operational implications of airway clearance systems for decision makers
Airway clearance systems have emerged as pivotal tools across respiratory care pathways, influencing clinical routines, home-care adoption, and multidisciplinary management of chronic secretion retention. Clinicians increasingly prioritize noninvasive techniques that reduce exacerbation risk, minimize caregiver burden, and integrate with telehealth monitoring, while device designers innovate to improve ease of use and adherence. As hospitals, clinics, and home-care providers re-evaluate treatment protocols, the role of airway clearance technologies in patient-centered care and resource optimization becomes more pronounced.
The landscape is shaped by converging forces: technological refinement of mechanical modalities, heightened emphasis on patient-reported outcomes, and an expanding recognition of the economic and human costs associated with ineffective secretion clearance. These factors collectively influence procurement decisions and clinical guidelines. Consequently, stakeholders require a concise, evidence-driven introduction that synthesizes clinical rationale, device characteristics, and operational considerations to inform strategy, procurement, and clinical adoption across care settings.
An incisive analysis of the transformative technological, clinical, and delivery model shifts reshaping adoption and strategic priorities for airway clearance solutions
The airway clearance sector is undergoing transformative shifts driven by device innovation, patient empowerment, and changes in care delivery models. Advanced oscillatory and percussive technologies have evolved from bulky clinical equipment to more user-friendly home devices, fostering longer-term adherence and enabling earlier intervention outside acute-care settings. Simultaneously, design emphasis on noise reduction, portability, and intuitive interfaces has broadened appeal among diverse patient cohorts, encouraging clinicians to incorporate a wider array of devices into individualized regimens.
Policy and reimbursement environments are also recalibrating clinical priorities, with payers and providers placing greater value on interventions that demonstrably reduce hospital readmissions and caregiver burden. The integration of airway clearance devices with remote monitoring platforms and digital therapeutics creates new pathways for adherence tracking and outcome measurement. As a result, manufacturers must align product development with interoperability expectations and clinical validation to remain competitive, while providers should incorporate device selection criteria that reflect long-term patient engagement and system-level efficiencies.
A comprehensive evaluation of the cumulative effects of 2025 tariff adjustments on procurement, sourcing strategies, and supply chain resilience across airway clearance device ecosystems
Tariff policy changes enacted in 2025 have introduced material complexity to procurement channels, supplier selection, and cross-border supply chains for airway clearance devices. Increased duties on certain medical device categories have prompted contracting teams to reassess vendor portfolios, prioritize localized manufacturing or regional distribution agreements, and renegotiate total landed cost assumptions. Procurement professionals are responding by exploring alternative sourcing routes, consolidating orders to leverage scale, and engaging in scenario planning to preserve continuity of supply while containing cost pressures.
The cumulative impact extends beyond direct unit costs to influence manufacturer pricing strategies, channel margins, and the comparative economics of refurbished or rental models. Regulatory compliance and documentation requirements tied to tariffs have also increased administrative overhead for cross-border shipments. In response, supply chain leaders and commercial teams are deepening collaboration to map value-chain exposure, implement hedging approaches where feasible, and communicate clearer cost-to-care trade-offs to clinical stakeholders. Ultimately, tariff-induced frictions are accelerating localized partnerships and compelling stakeholders to adopt procurement strategies that balance cost containment with clinical access.
A granular segmentation perspective that links device modalities, clinical indications, care settings, and distribution pathways to actionable product and commercialization strategies
Segmentation insights illuminate where clinical need, device innovation, and end-user preferences converge, providing a structured lens through which to assess product positioning and service delivery. Based on Device Type, market is studied across High Frequency Chest Wall Oscillation Device, Manual Chest Physiotherapy, Mechanical Vibrator, and Positive Expiratory Pressure Device. The Mechanical Vibrator is further studied across Automated Percussive Device and Handheld Mechanical Vibrator. The Positive Expiratory Pressure Device is further studied across Oscillating Positive Expiratory Pressure and Threshold Positive Expiratory Pressure. Each device class presents distinct usability considerations: chest wall oscillation systems emphasize caregiver-mediated therapy, manual physiotherapy relies on clinician skill and frequency of sessions, mechanical vibrators balance portability with percussive force, and positive expiratory pressure devices prioritize patient autonomy and breath-controlled efficacy.
Based on Indication, market is studied across Bronchiectasis, Chronic Obstructive Pulmonary Disease, Cystic Fibrosis, and Neuromuscular Disorders. These indications differ in secretion characteristics, frequency of exacerbations, and co-management needs, which in turn shape device selection criteria, clinician training requirements, and adherence support strategies. Based on End User, market is studied across Ambulatory Care Centers, Clinics, Home Care Settings, and Hospitals. Each care setting imposes unique constraints on device durability, cleaning protocols, and staff training pathways, as well as distinct reimbursement touchpoints. Based on Distribution Channel, market is studied across Direct Sales and Distributor Sales, which influence margin structures, field-level clinical education, and the speed at which innovations reach practitioners. Integrating these segmentation dimensions highlights opportunities for targeted R&D, differentiated commercial models, and tailored clinician engagement that reflect both clinical nuance and operational realities.
A strategic regional analysis linking regulatory nuance, reimbursement behavior, and adoption patterns across major geographies to inform localized market approaches
Regional dynamics shape regulatory pathways, reimbursement frameworks, and adoption velocities, requiring stakeholders to tailor strategies across geopolitical contexts. The Americas demonstrate diverse payer models and a strong focus on home-based care innovations, creating a favorable context for devices that marry ease of use with demonstrable patient adherence. Europe, Middle East & Africa present a heterogeneous regulatory and reimbursement landscape, with pockets of early clinical adoption alongside territories where procurement is centralized and price sensitivity is pronounced. The Asia-Pacific region is characterized by rapid infrastructure investment, growing home-care demand, and an expanding middle-class patient base that is receptive to portable, cost-effective devices.
These regional differences influence prioritization of clinical trials, postmarket surveillance efforts, and local manufacturing considerations. Supply chain and trade policies, as well as regional clinical guideline development, will further modulate device selection and reimbursement pathways. Consequently, commercial teams must develop region-specific value propositions and evidence packages that reflect each geography's regulatory expectations, clinician practice patterns, and payer priorities, while maintaining a coherent global brand and quality assurance framework.
An expert synthesis of competitive behaviors, innovation priorities, and strategic moves among leading manufacturers and service providers shaping the airway clearance ecosystem
Competitive dynamics in the airway clearance segment blend legacy medical-device incumbents with nimble innovators that emphasize user experience and digital integration. Key companies are investing in clinical evidence generation, postmarket data collection, and partnerships that extend device reach into home-care ecosystems and telehealth platforms. Strategic activity includes vertical integration of distribution, alliances with respiratory therapy networks, and incremental product enhancements that focus on noise reduction, portability, and adherence features.
Companies that demonstrate deep clinician engagement, robust training programs, and demonstrable impacts on patient-reported outcomes gain preferential access to hospital procurement committees and home-care ordering channels. Additionally, firms that align manufacturing footprints with tariff-affected routes and that can rapidly respond to supply-chain disruptions are better positioned to serve multinational customers. Effective commercialization hinges on balancing clinical validation with pragmatic considerations such as device lifecycle management, service offerings, and flexible pricing or rental models that reflect provider budget constraints and patient preferences.
Actionable recommendations for manufacturers, payers, and providers to enhance clinical adoption, supply resilience, and commercial performance in airway clearance solutions
Industry leaders should adopt a proactive posture that balances clinical credibility, supply chain resilience, and customer-centric commercialization. Prioritizing clinical evidence that links device use to reduced exacerbations and caregiver burden will strengthen reimbursement conversations and support adoption in both institutional and home-care settings. Manufacturers should also invest in product features that enhance adherence-such as simplified interfaces, quieter operation, and integrated digital adherence tracking-and align these innovations with clinician education programs to ensure effective deployment.
On the supply side, companies must diversify manufacturing and distribution footprints to mitigate tariff-driven cost volatility and ensure continuity of supply. Strategic distribution partnerships and localized assembly options can preserve competitiveness in sensitive jurisdictions. Commercial teams should refine go-to-market models to include flexible purchasing options, service and maintenance packages, and targeted clinician outreach that emphasizes outcomes rather than purely technical specifications. By integrating clinical evidence, customer experience enhancements, and supply-chain adaptability, leaders can capture long-term value while addressing short-term procurement pressures.
A transparent and reproducible research methodology combining clinical literature synthesis, stakeholder interviews, and supply-chain analysis to underpin authoritative insights
The research approach combined a structured review of peer-reviewed clinical literature, device registries, and regulatory filings with primary interviews conducted across clinical, procurement, and industry stakeholders. Evidence synthesis prioritized peer-reviewed clinical outcomes, real-world adherence studies, and regulatory guidance documents to ensure alignment with contemporary clinical practice and policy settings. Primary research included targeted discussions with respiratory therapists, hospital procurement officers, home-care coordinators, and product development leaders to capture operational constraints and real-world decision criteria.
Data validation steps incorporated cross-referencing of clinical claims with postmarket surveillance reports and manufacturer documentation, while thematic analysis distilled recurrent barriers and enablers of adoption. Tariff impact assessment drew on customs and trade policy releases and supply-chain practitioner interviews to map probable operational effects. The methodology was designed to emphasize triangulation across sources, transparent documentation of assumptions, and reproducibility of analytical steps to support confident interpretation by commercial and clinical stakeholders.
A concise conclusion synthesizing clinical significance, innovation trends, and strategic imperatives for stakeholders navigating the airway clearance sector
In conclusion, airway clearance systems occupy a strategic intersection of clinical need, patient empowerment, and evolving delivery models. The trajectory of device innovation favors portability, user-centric design, and digital integration, while health systems increasingly demand interventions that offer measurable reductions in exacerbations and caregiver burden. Tariff shifts and regional regulatory variability add complexity but also create incentives for localized manufacturing, strategic distribution partnerships, and evidence-driven value propositions.
For commercial and clinical leaders, the imperative is clear: align product development with robust clinical validation and clinician training, build supply-chain flexibility to navigate trade headwinds, and tailor regional strategies that reflect regulatory and payer realities. By doing so, stakeholders can advance patient outcomes while sustaining competitive positioning in a rapidly evolving landscape of airway clearance care.
Please Note: PDF & Excel + Online Access - 1 Year
A concise and authoritative introduction framing the clinical importance, technology evolution, and operational implications of airway clearance systems for decision makers
Airway clearance systems have emerged as pivotal tools across respiratory care pathways, influencing clinical routines, home-care adoption, and multidisciplinary management of chronic secretion retention. Clinicians increasingly prioritize noninvasive techniques that reduce exacerbation risk, minimize caregiver burden, and integrate with telehealth monitoring, while device designers innovate to improve ease of use and adherence. As hospitals, clinics, and home-care providers re-evaluate treatment protocols, the role of airway clearance technologies in patient-centered care and resource optimization becomes more pronounced.
The landscape is shaped by converging forces: technological refinement of mechanical modalities, heightened emphasis on patient-reported outcomes, and an expanding recognition of the economic and human costs associated with ineffective secretion clearance. These factors collectively influence procurement decisions and clinical guidelines. Consequently, stakeholders require a concise, evidence-driven introduction that synthesizes clinical rationale, device characteristics, and operational considerations to inform strategy, procurement, and clinical adoption across care settings.
An incisive analysis of the transformative technological, clinical, and delivery model shifts reshaping adoption and strategic priorities for airway clearance solutions
The airway clearance sector is undergoing transformative shifts driven by device innovation, patient empowerment, and changes in care delivery models. Advanced oscillatory and percussive technologies have evolved from bulky clinical equipment to more user-friendly home devices, fostering longer-term adherence and enabling earlier intervention outside acute-care settings. Simultaneously, design emphasis on noise reduction, portability, and intuitive interfaces has broadened appeal among diverse patient cohorts, encouraging clinicians to incorporate a wider array of devices into individualized regimens.
Policy and reimbursement environments are also recalibrating clinical priorities, with payers and providers placing greater value on interventions that demonstrably reduce hospital readmissions and caregiver burden. The integration of airway clearance devices with remote monitoring platforms and digital therapeutics creates new pathways for adherence tracking and outcome measurement. As a result, manufacturers must align product development with interoperability expectations and clinical validation to remain competitive, while providers should incorporate device selection criteria that reflect long-term patient engagement and system-level efficiencies.
A comprehensive evaluation of the cumulative effects of 2025 tariff adjustments on procurement, sourcing strategies, and supply chain resilience across airway clearance device ecosystems
Tariff policy changes enacted in 2025 have introduced material complexity to procurement channels, supplier selection, and cross-border supply chains for airway clearance devices. Increased duties on certain medical device categories have prompted contracting teams to reassess vendor portfolios, prioritize localized manufacturing or regional distribution agreements, and renegotiate total landed cost assumptions. Procurement professionals are responding by exploring alternative sourcing routes, consolidating orders to leverage scale, and engaging in scenario planning to preserve continuity of supply while containing cost pressures.
The cumulative impact extends beyond direct unit costs to influence manufacturer pricing strategies, channel margins, and the comparative economics of refurbished or rental models. Regulatory compliance and documentation requirements tied to tariffs have also increased administrative overhead for cross-border shipments. In response, supply chain leaders and commercial teams are deepening collaboration to map value-chain exposure, implement hedging approaches where feasible, and communicate clearer cost-to-care trade-offs to clinical stakeholders. Ultimately, tariff-induced frictions are accelerating localized partnerships and compelling stakeholders to adopt procurement strategies that balance cost containment with clinical access.
A granular segmentation perspective that links device modalities, clinical indications, care settings, and distribution pathways to actionable product and commercialization strategies
Segmentation insights illuminate where clinical need, device innovation, and end-user preferences converge, providing a structured lens through which to assess product positioning and service delivery. Based on Device Type, market is studied across High Frequency Chest Wall Oscillation Device, Manual Chest Physiotherapy, Mechanical Vibrator, and Positive Expiratory Pressure Device. The Mechanical Vibrator is further studied across Automated Percussive Device and Handheld Mechanical Vibrator. The Positive Expiratory Pressure Device is further studied across Oscillating Positive Expiratory Pressure and Threshold Positive Expiratory Pressure. Each device class presents distinct usability considerations: chest wall oscillation systems emphasize caregiver-mediated therapy, manual physiotherapy relies on clinician skill and frequency of sessions, mechanical vibrators balance portability with percussive force, and positive expiratory pressure devices prioritize patient autonomy and breath-controlled efficacy.
Based on Indication, market is studied across Bronchiectasis, Chronic Obstructive Pulmonary Disease, Cystic Fibrosis, and Neuromuscular Disorders. These indications differ in secretion characteristics, frequency of exacerbations, and co-management needs, which in turn shape device selection criteria, clinician training requirements, and adherence support strategies. Based on End User, market is studied across Ambulatory Care Centers, Clinics, Home Care Settings, and Hospitals. Each care setting imposes unique constraints on device durability, cleaning protocols, and staff training pathways, as well as distinct reimbursement touchpoints. Based on Distribution Channel, market is studied across Direct Sales and Distributor Sales, which influence margin structures, field-level clinical education, and the speed at which innovations reach practitioners. Integrating these segmentation dimensions highlights opportunities for targeted R&D, differentiated commercial models, and tailored clinician engagement that reflect both clinical nuance and operational realities.
A strategic regional analysis linking regulatory nuance, reimbursement behavior, and adoption patterns across major geographies to inform localized market approaches
Regional dynamics shape regulatory pathways, reimbursement frameworks, and adoption velocities, requiring stakeholders to tailor strategies across geopolitical contexts. The Americas demonstrate diverse payer models and a strong focus on home-based care innovations, creating a favorable context for devices that marry ease of use with demonstrable patient adherence. Europe, Middle East & Africa present a heterogeneous regulatory and reimbursement landscape, with pockets of early clinical adoption alongside territories where procurement is centralized and price sensitivity is pronounced. The Asia-Pacific region is characterized by rapid infrastructure investment, growing home-care demand, and an expanding middle-class patient base that is receptive to portable, cost-effective devices.
These regional differences influence prioritization of clinical trials, postmarket surveillance efforts, and local manufacturing considerations. Supply chain and trade policies, as well as regional clinical guideline development, will further modulate device selection and reimbursement pathways. Consequently, commercial teams must develop region-specific value propositions and evidence packages that reflect each geography's regulatory expectations, clinician practice patterns, and payer priorities, while maintaining a coherent global brand and quality assurance framework.
An expert synthesis of competitive behaviors, innovation priorities, and strategic moves among leading manufacturers and service providers shaping the airway clearance ecosystem
Competitive dynamics in the airway clearance segment blend legacy medical-device incumbents with nimble innovators that emphasize user experience and digital integration. Key companies are investing in clinical evidence generation, postmarket data collection, and partnerships that extend device reach into home-care ecosystems and telehealth platforms. Strategic activity includes vertical integration of distribution, alliances with respiratory therapy networks, and incremental product enhancements that focus on noise reduction, portability, and adherence features.
Companies that demonstrate deep clinician engagement, robust training programs, and demonstrable impacts on patient-reported outcomes gain preferential access to hospital procurement committees and home-care ordering channels. Additionally, firms that align manufacturing footprints with tariff-affected routes and that can rapidly respond to supply-chain disruptions are better positioned to serve multinational customers. Effective commercialization hinges on balancing clinical validation with pragmatic considerations such as device lifecycle management, service offerings, and flexible pricing or rental models that reflect provider budget constraints and patient preferences.
Actionable recommendations for manufacturers, payers, and providers to enhance clinical adoption, supply resilience, and commercial performance in airway clearance solutions
Industry leaders should adopt a proactive posture that balances clinical credibility, supply chain resilience, and customer-centric commercialization. Prioritizing clinical evidence that links device use to reduced exacerbations and caregiver burden will strengthen reimbursement conversations and support adoption in both institutional and home-care settings. Manufacturers should also invest in product features that enhance adherence-such as simplified interfaces, quieter operation, and integrated digital adherence tracking-and align these innovations with clinician education programs to ensure effective deployment.
On the supply side, companies must diversify manufacturing and distribution footprints to mitigate tariff-driven cost volatility and ensure continuity of supply. Strategic distribution partnerships and localized assembly options can preserve competitiveness in sensitive jurisdictions. Commercial teams should refine go-to-market models to include flexible purchasing options, service and maintenance packages, and targeted clinician outreach that emphasizes outcomes rather than purely technical specifications. By integrating clinical evidence, customer experience enhancements, and supply-chain adaptability, leaders can capture long-term value while addressing short-term procurement pressures.
A transparent and reproducible research methodology combining clinical literature synthesis, stakeholder interviews, and supply-chain analysis to underpin authoritative insights
The research approach combined a structured review of peer-reviewed clinical literature, device registries, and regulatory filings with primary interviews conducted across clinical, procurement, and industry stakeholders. Evidence synthesis prioritized peer-reviewed clinical outcomes, real-world adherence studies, and regulatory guidance documents to ensure alignment with contemporary clinical practice and policy settings. Primary research included targeted discussions with respiratory therapists, hospital procurement officers, home-care coordinators, and product development leaders to capture operational constraints and real-world decision criteria.
Data validation steps incorporated cross-referencing of clinical claims with postmarket surveillance reports and manufacturer documentation, while thematic analysis distilled recurrent barriers and enablers of adoption. Tariff impact assessment drew on customs and trade policy releases and supply-chain practitioner interviews to map probable operational effects. The methodology was designed to emphasize triangulation across sources, transparent documentation of assumptions, and reproducibility of analytical steps to support confident interpretation by commercial and clinical stakeholders.
A concise conclusion synthesizing clinical significance, innovation trends, and strategic imperatives for stakeholders navigating the airway clearance sector
In conclusion, airway clearance systems occupy a strategic intersection of clinical need, patient empowerment, and evolving delivery models. The trajectory of device innovation favors portability, user-centric design, and digital integration, while health systems increasingly demand interventions that offer measurable reductions in exacerbations and caregiver burden. Tariff shifts and regional regulatory variability add complexity but also create incentives for localized manufacturing, strategic distribution partnerships, and evidence-driven value propositions.
For commercial and clinical leaders, the imperative is clear: align product development with robust clinical validation and clinician training, build supply-chain flexibility to navigate trade headwinds, and tailor regional strategies that reflect regulatory and payer realities. By doing so, stakeholders can advance patient outcomes while sustaining competitive positioning in a rapidly evolving landscape of airway clearance care.
Please Note: PDF & Excel + Online Access - 1 Year
Table of Contents
196 Pages
- 1. Preface
- 1.1. Objectives of the Study
- 1.2. Market Segmentation & Coverage
- 1.3. Years Considered for the Study
- 1.4. Currency
- 1.5. Language
- 1.6. Stakeholders
- 2. Research Methodology
- 3. Executive Summary
- 4. Market Overview
- 5. Market Insights
- 5.1. Growing demand for wearable vibratory vest systems enabling at-home respiratory therapy sessions for chronic patients
- 5.2. Increasing integration of digital connectivity and mobile apps in airway clearance devices for real-time patient monitoring
- 5.3. Rising preference for portable handheld oscillating positive expiratory pressure devices among COPD and cystic fibrosis patients
- 5.4. Advancements in low-frequency chest wall compression technologies improving secretion clearance efficacy and patient comfort
- 5.5. Expansion of telehealth-compatible airway clearance platforms facilitating remote clinician supervision and adherence tracking
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Airway Clearance System Market, by Device Type
- 8.1. High Frequency Chest Wall Oscillation Device
- 8.2. Manual Chest Physiotherapy
- 8.3. Mechanical Vibrator
- 8.3.1. Automated Percussive Device
- 8.3.2. Handheld Mechanical Vibrator
- 8.4. Positive Expiratory Pressure Device
- 8.4.1. Oscillating Positive Expiratory Pressure
- 8.4.2. Threshold Positive Expiratory Pressure
- 9. Airway Clearance System Market, by Indication
- 9.1. Bronchiectasis
- 9.2. Chronic Obstructive Pulmonary Disease
- 9.3. Cystic Fibrosis
- 9.4. Neuromuscular Disorders
- 10. Airway Clearance System Market, by End User
- 10.1. Ambulatory Care Centers
- 10.2. Clinics
- 10.3. Home Care Settings
- 10.4. Hospitals
- 11. Airway Clearance System Market, by Distribution Channel
- 11.1. Direct Sales
- 11.2. Distributor Sales
- 12. Airway Clearance System Market, by Region
- 12.1. Americas
- 12.1.1. North America
- 12.1.2. Latin America
- 12.2. Europe, Middle East & Africa
- 12.2.1. Europe
- 12.2.2. Middle East
- 12.2.3. Africa
- 12.3. Asia-Pacific
- 13. Airway Clearance System Market, by Group
- 13.1. ASEAN
- 13.2. GCC
- 13.3. European Union
- 13.4. BRICS
- 13.5. G7
- 13.6. NATO
- 14. Airway Clearance System Market, by Country
- 14.1. United States
- 14.2. Canada
- 14.3. Mexico
- 14.4. Brazil
- 14.5. United Kingdom
- 14.6. Germany
- 14.7. France
- 14.8. Russia
- 14.9. Italy
- 14.10. Spain
- 14.11. China
- 14.12. India
- 14.13. Japan
- 14.14. Australia
- 14.15. South Korea
- 15. Competitive Landscape
- 15.1. Market Share Analysis, 2024
- 15.2. FPNV Positioning Matrix, 2024
- 15.3. Competitive Analysis
- 15.3.1. Baxter International Inc.
- 15.3.2. Koninklijke Philips N.V.
- 15.3.3. Medtronic plc
- 15.3.4. General Electric Company
- 15.3.5. Smiths Group plc
- 15.3.6. Invacare Corporation
- 15.3.7. Becton, Dickinson and Company
- 15.3.8. Drägerwerk AG & Co. KGaA
- 15.3.9. Monaghan Medical Corporation
- 15.3.10. PARI GmbH
- 15.3.11. International Biophysics Corporation
- 15.3.12. Hill-Rom Holdings, Inc.
- 15.3.13. Dymedso, Inc.
- 15.3.14. Respiratory Technologies, Inc.
- 15.3.15. Thayer Medical, Inc.
- 15.3.16. VORTRAN Medical Technology, Inc.
- 15.3.17. Med Systems, Inc.
- 15.3.18. General Physiotherapy II LLC
- 15.3.19. AbbVie Inc.
- 15.3.20. VYAIRE Medical Inc
- 15.3.21. Westmed, Inc.
- 15.3.22. Medicare Equipment & Supplies, Inc.
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