Gravity Ridge Ventilators Market by Product Type (Home Use, Intensive Care, Transport), Operation Mode (Invasive, Non Invasive), Portability, End User, Distribution Channel - Global Forecast 2026-2032
Description
The Gravity Ridge Ventilators Market was valued at USD 5.56 billion in 2025 and is projected to grow to USD 5.80 billion in 2026, with a CAGR of 4.46%, reaching USD 7.55 billion by 2032.
A succinct overview of the evolving clinical, technological, and supply chain influences reshaping ventilator priorities across care settings
The landscape of gravity ridge ventilators is evolving rapidly as clinical demands, regulatory expectations, and supply chain dynamics converge. Advances in ventilator technology, coupled with heightened awareness of respiratory care continuity outside traditional hospital settings, have elevated the importance of device versatility and reliability. Consequently, stakeholders across clinical, procurement, and manufacturing domains are recalibrating priorities to balance high-acuity performance with portability, intuitive user interfaces, and streamlined maintenance protocols.
Emerging use cases now prioritize hybrid care settings where devices must smoothly transition between intensive care, transport, and home environments without compromising safety. Interoperability with electronic health records and remote monitoring platforms is increasingly central to procurement decisions. At the same time, manufacturers face pressure to maintain resilient supply chains, adopt modular designs that simplify servicing, and support training frameworks that reduce operational risk. These factors collectively shape strategic choices about product development, commercialization, and partnerships.
How clinical decentralization, digital integration, regulatory tightening, and service-oriented buying are fundamentally altering ventilator design and commercialization
Transformative shifts are visible across clinical practice and device innovation as emphasis moves from single-setting performance to cross-setting adaptability. Pressure toward decentralized care models has pushed non-invasive ventilation technologies into more diverse contexts, while invasive ventilation systems have been refined to offer clearer modes and safeguards for complex patient populations. Simultaneously, digital integration and sensor-driven automation have reduced clinician workload by enabling smarter alarm management, predictive maintenance alerts, and context-aware control algorithms.
In parallel, procurement and reimbursement structures are adapting to support lifecycle value rather than upfront acquisition cost alone. This recalibration encourages subscription-style service models and greater OEM involvement in post-sale support. Regulatory authorities are responding by tightening requirements for software validation, cybersecurity protections, and human factors engineering, prompting manufacturers to invest earlier in compliance-driven design. These shifts collectively create a higher bar for usability, reliability, and long-term operational sustainability.
The 2025 tariff landscape and its strategic implications for global sourcing, aftermarket resilience, and localized production strategies in ventilator supply chains
Recent tariff policies imposed by the United States in 2025 have added a new layer of complexity to global ventilator supply chains and procurement strategies. These measures have amplified the need for manufacturers and suppliers to rethink sourcing footprints, localize critical component production, and diversify logistics pathways to mitigate exposure to tariff-induced cost volatility. As a result, decision-makers are prioritizing supplier relationships that can demonstrate tariff resilience through multi-jurisdictional production or established bonded inventory mechanisms.
Beyond cost implications, tariffs have also influenced network design for aftermarket support and spare part provisioning. Healthcare providers and OEMs are exploring regionalized spare-part depots and third-party service partnerships to reduce lead times and avoid cross-border duties during urgent replacements. At the same time, tariff-driven shifting of production has accelerated conversations about nearshoring and strategic partnerships that preserve quality control while reducing customs risk. Ultimately, this environment favors organizations with flexible manufacturing capabilities and adaptive commercial models that absorb regulatory shifts without compromising device availability.
Detailed segmentation insights showing how operation modes, product types, portability choices, end-user expectations, and distribution channels shape design and commercialization strategies
A granular segmentation-based understanding of ventilator demand and operational requirements reveals distinct development and commercialization pathways. When assessed by operation mode, the market divides into invasive systems, which include pressure ventilation and volume ventilation subtypes tailored for controlled clinical environments, and non-invasive systems, which encompass bilevel positive airway pressure and continuous positive airway pressure modalities ideal for ambulatory and home-care contexts. This distinction drives divergent engineering priorities: invasive devices emphasize precise control algorithms and multi-parameter monitoring, whereas non-invasive devices prioritize patient comfort, noise reduction, and simplified interfaces.
Product type segmentation further clarifies design trade-offs, distinguishing home use devices, intensive care platforms that address both adult and neonatal/pediatric care requirements, and transport solutions that must withstand environmental variability and vibration. Portability segmentation differentiates between portable units-available as handheld or trolley-mounted forms-and stationary installations, informing battery management strategies, ruggedization, and maintenance access. End-user segmentation exposes varied procurement and usage patterns across ambulatory centers, homecare settings, and hospitals, with hospitals further split into government and private entities that follow distinct purchasing protocols and service expectations. Finally, distribution channel classification into direct sales, distributor partnerships, and online retail highlights the need for tailored commercial and after-sales pathways that accommodate clinical procurement cycles, regulatory documentation requirements, and consumer-facing education. Taken together, these segmentation lenses enable product teams to align feature sets, certification pathways, and support models with the nuanced needs of each user group and care environment.
Cross-regional strategic perspectives highlighting how the Americas, Europe Middle East & Africa, and Asia-Pacific require distinct regulatory, manufacturing, and commercialization approaches
Regional dynamics play a decisive role in regulatory priorities, clinical adoption patterns, and procurement norms for ventilators. In the Americas, health systems emphasize integration with acute care protocols and scalable service models that support both large hospital networks and distributed community care. This region typically expects robust post-sale support and clear interoperability standards, which influence device connectivity requirements and maintenance offers.
Across Europe, the Middle East & Africa, regulatory harmonization efforts and diverse payer landscapes create a mosaic of certification and reimbursement considerations. Manufacturers must navigate varying approval pathways and align device features with localized clinical guidelines. In the Asia-Pacific region, rapid expansion of homecare infrastructure, substantial investments in public health capacity, and an emphasis on cost-effective manufacturing drive demand for adaptable devices that can be deployed in both high-acuity and resource-constrained settings. Each region therefore warrants tailored regulatory strategies, manufacturing footprints, and commercial approaches to optimize device adoption and lifecycle support.
What separates leading ventilator manufacturers today is their convergence of proven clinical performance, resilient supply networks, and integrated digital service offerings
Competitive positioning among leading ventilator companies is increasingly defined by three core capabilities: clinical validation and usability, supply chain resilience, and digital service ecosystems. Organizations that excel at deep clinical partnerships and rigorous usability testing tend to achieve stronger acceptance in intensive care and neonatal/pediatric applications. Conversely, firms that invest in modular hardware and scalable manufacturing platforms can respond more rapidly to shifts in demand and regulatory changes.
Moreover, differentiated aftermarket services-ranging from remote monitoring and predictive maintenance to expedited spare-part delivery networks-are becoming essential differentiators. Strategic alliances with logistics providers and third-party servicing organizations provide quicker field response times and lower total ownership friction. Finally, the ability to offer comprehensive training and certification for clinical users across multiple care settings strengthens adoption and reduces implementation risk, particularly when devices cross boundaries between hospital, transport, and home environments.
Actionable strategies for manufacturers and healthcare leaders to build modular products, enhance supply resilience, and align commercial models with diverse care settings
Industry leaders must adopt a multi-pronged approach that balances engineering rigor with commercial agility to remain competitive. First, investing in modular platform architectures enables rapid configuration for invasive or non-invasive applications while simplifying regulatory submissions and aftermarket servicing. This approach reduces time to deployment across product type variants and supports consistency in clinical performance expectations.
Second, establishing geographically distributed manufacturing or strategic nearshoring partnerships will mitigate tariff exposure and logistics disruptions, while regional spare-part hubs can ensure continuity of care during urgent replacements. Third, embedding cybersecurity, software lifecycle management, and human factors engineering into product roadmaps will satisfy evolving regulatory scrutiny and improve clinician trust. Finally, developing flexible commercial models-including bundled service agreements and targeted training programs for hospitals, ambulatory centers, and homecare providers-will help align device value propositions with purchaser priorities and accelerate adoption across diverse end users.
A rigorous, multi-source methodology combining stakeholder interviews, technical validation, regulatory review, and supply chain scenario analysis to ensure actionable insights
The research underpinning this summary integrates primary stakeholder interviews, technical device assessments, regulatory reviews, and supply chain analysis to construct a comprehensive perspective on ventilator dynamics. Primary insights were gathered through structured discussions with clinicians, biomedical engineers, procurement specialists, and aftermarket service providers to capture use-case requirements, usability concerns, and lifecycle support expectations. These qualitative inputs were complemented by systematic reviews of regulatory guidance, technical white papers, and device specifications to validate performance claims and identify prevailing design patterns.
Supply chain evaluations incorporated component availability checks, logistical pathway mapping, and scenario analysis to assess tariff sensitivity and manufacturing flexibility. Competitive profiling relied on public regulatory filings, product documentation, and service offerings to deduce positioning themes without relying on proprietary market estimates. Throughout, the methodology emphasized triangulation across independent sources to ensure robustness and practical relevance for decision-makers seeking to align product strategy with clinical needs, regulatory realities, and operational constraints.
Conclusive perspectives on how integrated product, regulatory, and supply strategies enable sustainable ventilator deployment across diverse care pathways
In conclusion, the gravity ridge ventilator landscape is shaped by intersecting forces of clinical decentralization, technological integration, and geopolitical trade considerations. Stakeholders that prioritize modular design, strong clinician engagement, and regional supply chain resilience are best positioned to navigate tariff fluctuations, regulatory complexity, and shifting care delivery models. Equally important is the provision of comprehensive aftermarket services and training programs that reduce operational risk and improve clinical outcomes during device deployment across hospitals, transport scenarios, and homecare settings.
Moving forward, organizations should treat device strategy as an ecosystem challenge that requires coordinated investments across engineering, regulatory affairs, manufacturing, and commercial teams. By aligning product capabilities with real-world workflows and regional requirements, manufacturers and health systems can accelerate safe adoption and ensure that ventilator solutions deliver consistent value across diverse patient populations and care environments.
Note: PDF & Excel + Online Access - 1 Year
A succinct overview of the evolving clinical, technological, and supply chain influences reshaping ventilator priorities across care settings
The landscape of gravity ridge ventilators is evolving rapidly as clinical demands, regulatory expectations, and supply chain dynamics converge. Advances in ventilator technology, coupled with heightened awareness of respiratory care continuity outside traditional hospital settings, have elevated the importance of device versatility and reliability. Consequently, stakeholders across clinical, procurement, and manufacturing domains are recalibrating priorities to balance high-acuity performance with portability, intuitive user interfaces, and streamlined maintenance protocols.
Emerging use cases now prioritize hybrid care settings where devices must smoothly transition between intensive care, transport, and home environments without compromising safety. Interoperability with electronic health records and remote monitoring platforms is increasingly central to procurement decisions. At the same time, manufacturers face pressure to maintain resilient supply chains, adopt modular designs that simplify servicing, and support training frameworks that reduce operational risk. These factors collectively shape strategic choices about product development, commercialization, and partnerships.
How clinical decentralization, digital integration, regulatory tightening, and service-oriented buying are fundamentally altering ventilator design and commercialization
Transformative shifts are visible across clinical practice and device innovation as emphasis moves from single-setting performance to cross-setting adaptability. Pressure toward decentralized care models has pushed non-invasive ventilation technologies into more diverse contexts, while invasive ventilation systems have been refined to offer clearer modes and safeguards for complex patient populations. Simultaneously, digital integration and sensor-driven automation have reduced clinician workload by enabling smarter alarm management, predictive maintenance alerts, and context-aware control algorithms.
In parallel, procurement and reimbursement structures are adapting to support lifecycle value rather than upfront acquisition cost alone. This recalibration encourages subscription-style service models and greater OEM involvement in post-sale support. Regulatory authorities are responding by tightening requirements for software validation, cybersecurity protections, and human factors engineering, prompting manufacturers to invest earlier in compliance-driven design. These shifts collectively create a higher bar for usability, reliability, and long-term operational sustainability.
The 2025 tariff landscape and its strategic implications for global sourcing, aftermarket resilience, and localized production strategies in ventilator supply chains
Recent tariff policies imposed by the United States in 2025 have added a new layer of complexity to global ventilator supply chains and procurement strategies. These measures have amplified the need for manufacturers and suppliers to rethink sourcing footprints, localize critical component production, and diversify logistics pathways to mitigate exposure to tariff-induced cost volatility. As a result, decision-makers are prioritizing supplier relationships that can demonstrate tariff resilience through multi-jurisdictional production or established bonded inventory mechanisms.
Beyond cost implications, tariffs have also influenced network design for aftermarket support and spare part provisioning. Healthcare providers and OEMs are exploring regionalized spare-part depots and third-party service partnerships to reduce lead times and avoid cross-border duties during urgent replacements. At the same time, tariff-driven shifting of production has accelerated conversations about nearshoring and strategic partnerships that preserve quality control while reducing customs risk. Ultimately, this environment favors organizations with flexible manufacturing capabilities and adaptive commercial models that absorb regulatory shifts without compromising device availability.
Detailed segmentation insights showing how operation modes, product types, portability choices, end-user expectations, and distribution channels shape design and commercialization strategies
A granular segmentation-based understanding of ventilator demand and operational requirements reveals distinct development and commercialization pathways. When assessed by operation mode, the market divides into invasive systems, which include pressure ventilation and volume ventilation subtypes tailored for controlled clinical environments, and non-invasive systems, which encompass bilevel positive airway pressure and continuous positive airway pressure modalities ideal for ambulatory and home-care contexts. This distinction drives divergent engineering priorities: invasive devices emphasize precise control algorithms and multi-parameter monitoring, whereas non-invasive devices prioritize patient comfort, noise reduction, and simplified interfaces.
Product type segmentation further clarifies design trade-offs, distinguishing home use devices, intensive care platforms that address both adult and neonatal/pediatric care requirements, and transport solutions that must withstand environmental variability and vibration. Portability segmentation differentiates between portable units-available as handheld or trolley-mounted forms-and stationary installations, informing battery management strategies, ruggedization, and maintenance access. End-user segmentation exposes varied procurement and usage patterns across ambulatory centers, homecare settings, and hospitals, with hospitals further split into government and private entities that follow distinct purchasing protocols and service expectations. Finally, distribution channel classification into direct sales, distributor partnerships, and online retail highlights the need for tailored commercial and after-sales pathways that accommodate clinical procurement cycles, regulatory documentation requirements, and consumer-facing education. Taken together, these segmentation lenses enable product teams to align feature sets, certification pathways, and support models with the nuanced needs of each user group and care environment.
Cross-regional strategic perspectives highlighting how the Americas, Europe Middle East & Africa, and Asia-Pacific require distinct regulatory, manufacturing, and commercialization approaches
Regional dynamics play a decisive role in regulatory priorities, clinical adoption patterns, and procurement norms for ventilators. In the Americas, health systems emphasize integration with acute care protocols and scalable service models that support both large hospital networks and distributed community care. This region typically expects robust post-sale support and clear interoperability standards, which influence device connectivity requirements and maintenance offers.
Across Europe, the Middle East & Africa, regulatory harmonization efforts and diverse payer landscapes create a mosaic of certification and reimbursement considerations. Manufacturers must navigate varying approval pathways and align device features with localized clinical guidelines. In the Asia-Pacific region, rapid expansion of homecare infrastructure, substantial investments in public health capacity, and an emphasis on cost-effective manufacturing drive demand for adaptable devices that can be deployed in both high-acuity and resource-constrained settings. Each region therefore warrants tailored regulatory strategies, manufacturing footprints, and commercial approaches to optimize device adoption and lifecycle support.
What separates leading ventilator manufacturers today is their convergence of proven clinical performance, resilient supply networks, and integrated digital service offerings
Competitive positioning among leading ventilator companies is increasingly defined by three core capabilities: clinical validation and usability, supply chain resilience, and digital service ecosystems. Organizations that excel at deep clinical partnerships and rigorous usability testing tend to achieve stronger acceptance in intensive care and neonatal/pediatric applications. Conversely, firms that invest in modular hardware and scalable manufacturing platforms can respond more rapidly to shifts in demand and regulatory changes.
Moreover, differentiated aftermarket services-ranging from remote monitoring and predictive maintenance to expedited spare-part delivery networks-are becoming essential differentiators. Strategic alliances with logistics providers and third-party servicing organizations provide quicker field response times and lower total ownership friction. Finally, the ability to offer comprehensive training and certification for clinical users across multiple care settings strengthens adoption and reduces implementation risk, particularly when devices cross boundaries between hospital, transport, and home environments.
Actionable strategies for manufacturers and healthcare leaders to build modular products, enhance supply resilience, and align commercial models with diverse care settings
Industry leaders must adopt a multi-pronged approach that balances engineering rigor with commercial agility to remain competitive. First, investing in modular platform architectures enables rapid configuration for invasive or non-invasive applications while simplifying regulatory submissions and aftermarket servicing. This approach reduces time to deployment across product type variants and supports consistency in clinical performance expectations.
Second, establishing geographically distributed manufacturing or strategic nearshoring partnerships will mitigate tariff exposure and logistics disruptions, while regional spare-part hubs can ensure continuity of care during urgent replacements. Third, embedding cybersecurity, software lifecycle management, and human factors engineering into product roadmaps will satisfy evolving regulatory scrutiny and improve clinician trust. Finally, developing flexible commercial models-including bundled service agreements and targeted training programs for hospitals, ambulatory centers, and homecare providers-will help align device value propositions with purchaser priorities and accelerate adoption across diverse end users.
A rigorous, multi-source methodology combining stakeholder interviews, technical validation, regulatory review, and supply chain scenario analysis to ensure actionable insights
The research underpinning this summary integrates primary stakeholder interviews, technical device assessments, regulatory reviews, and supply chain analysis to construct a comprehensive perspective on ventilator dynamics. Primary insights were gathered through structured discussions with clinicians, biomedical engineers, procurement specialists, and aftermarket service providers to capture use-case requirements, usability concerns, and lifecycle support expectations. These qualitative inputs were complemented by systematic reviews of regulatory guidance, technical white papers, and device specifications to validate performance claims and identify prevailing design patterns.
Supply chain evaluations incorporated component availability checks, logistical pathway mapping, and scenario analysis to assess tariff sensitivity and manufacturing flexibility. Competitive profiling relied on public regulatory filings, product documentation, and service offerings to deduce positioning themes without relying on proprietary market estimates. Throughout, the methodology emphasized triangulation across independent sources to ensure robustness and practical relevance for decision-makers seeking to align product strategy with clinical needs, regulatory realities, and operational constraints.
Conclusive perspectives on how integrated product, regulatory, and supply strategies enable sustainable ventilator deployment across diverse care pathways
In conclusion, the gravity ridge ventilator landscape is shaped by intersecting forces of clinical decentralization, technological integration, and geopolitical trade considerations. Stakeholders that prioritize modular design, strong clinician engagement, and regional supply chain resilience are best positioned to navigate tariff fluctuations, regulatory complexity, and shifting care delivery models. Equally important is the provision of comprehensive aftermarket services and training programs that reduce operational risk and improve clinical outcomes during device deployment across hospitals, transport scenarios, and homecare settings.
Moving forward, organizations should treat device strategy as an ecosystem challenge that requires coordinated investments across engineering, regulatory affairs, manufacturing, and commercial teams. By aligning product capabilities with real-world workflows and regional requirements, manufacturers and health systems can accelerate safe adoption and ensure that ventilator solutions deliver consistent value across diverse patient populations and care environments.
Note: PDF & Excel + Online Access - 1 Year
Table of Contents
194 Pages
- 1. Preface
- 1.1. Objectives of the Study
- 1.2. Market Definition
- 1.3. Market Segmentation & Coverage
- 1.4. Years Considered for the Study
- 1.5. Currency Considered for the Study
- 1.6. Language Considered for the Study
- 1.7. Key Stakeholders
- 2. Research Methodology
- 2.1. Introduction
- 2.2. Research Design
- 2.2.1. Primary Research
- 2.2.2. Secondary Research
- 2.3. Research Framework
- 2.3.1. Qualitative Analysis
- 2.3.2. Quantitative Analysis
- 2.4. Market Size Estimation
- 2.4.1. Top-Down Approach
- 2.4.2. Bottom-Up Approach
- 2.5. Data Triangulation
- 2.6. Research Outcomes
- 2.7. Research Assumptions
- 2.8. Research Limitations
- 3. Executive Summary
- 3.1. Introduction
- 3.2. CXO Perspective
- 3.3. Market Size & Growth Trends
- 3.4. Market Share Analysis, 2025
- 3.5. FPNV Positioning Matrix, 2025
- 3.6. New Revenue Opportunities
- 3.7. Next-Generation Business Models
- 3.8. Industry Roadmap
- 4. Market Overview
- 4.1. Introduction
- 4.2. Industry Ecosystem & Value Chain Analysis
- 4.2.1. Supply-Side Analysis
- 4.2.2. Demand-Side Analysis
- 4.2.3. Stakeholder Analysis
- 4.3. Porter’s Five Forces Analysis
- 4.4. PESTLE Analysis
- 4.5. Market Outlook
- 4.5.1. Near-Term Market Outlook (0–2 Years)
- 4.5.2. Medium-Term Market Outlook (3–5 Years)
- 4.5.3. Long-Term Market Outlook (5–10 Years)
- 4.6. Go-to-Market Strategy
- 5. Market Insights
- 5.1. Consumer Insights & End-User Perspective
- 5.2. Consumer Experience Benchmarking
- 5.3. Opportunity Mapping
- 5.4. Distribution Channel Analysis
- 5.5. Pricing Trend Analysis
- 5.6. Regulatory Compliance & Standards Framework
- 5.7. ESG & Sustainability Analysis
- 5.8. Disruption & Risk Scenarios
- 5.9. Return on Investment & Cost-Benefit Analysis
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Gravity Ridge Ventilators Market, by Product Type
- 8.1. Home Use
- 8.2. Intensive Care
- 8.2.1. Adult
- 8.2.2. Neonatal/Pediatric
- 8.3. Transport
- 9. Gravity Ridge Ventilators Market, by Operation Mode
- 9.1. Invasive
- 9.1.1. Pressure Ventilation
- 9.1.2. Volume Ventilation
- 9.2. Non Invasive
- 9.2.1. Bilevel Positive Airway Pressure
- 9.2.2. Continuous Positive Airway Pressure
- 10. Gravity Ridge Ventilators Market, by Portability
- 10.1. Portable
- 10.1.1. Handheld
- 10.1.2. Trolley Mounted
- 10.2. Stationary
- 11. Gravity Ridge Ventilators Market, by End User
- 11.1. Ambulatory Centers
- 11.2. Homecare Settings
- 11.3. Hospitals
- 11.3.1. Government
- 11.3.2. Private
- 12. Gravity Ridge Ventilators Market, by Distribution Channel
- 12.1. Direct
- 12.2. Distributor
- 12.3. Online Retail
- 13. Gravity Ridge Ventilators Market, by Region
- 13.1. Americas
- 13.1.1. North America
- 13.1.2. Latin America
- 13.2. Europe, Middle East & Africa
- 13.2.1. Europe
- 13.2.2. Middle East
- 13.2.3. Africa
- 13.3. Asia-Pacific
- 14. Gravity Ridge Ventilators Market, by Group
- 14.1. ASEAN
- 14.2. GCC
- 14.3. European Union
- 14.4. BRICS
- 14.5. G7
- 14.6. NATO
- 15. Gravity Ridge Ventilators Market, by Country
- 15.1. United States
- 15.2. Canada
- 15.3. Mexico
- 15.4. Brazil
- 15.5. United Kingdom
- 15.6. Germany
- 15.7. France
- 15.8. Russia
- 15.9. Italy
- 15.10. Spain
- 15.11. China
- 15.12. India
- 15.13. Japan
- 15.14. Australia
- 15.15. South Korea
- 16. United States Gravity Ridge Ventilators Market
- 17. China Gravity Ridge Ventilators Market
- 18. Competitive Landscape
- 18.1. Market Concentration Analysis, 2025
- 18.1.1. Concentration Ratio (CR)
- 18.1.2. Herfindahl Hirschman Index (HHI)
- 18.2. Recent Developments & Impact Analysis, 2025
- 18.3. Product Portfolio Analysis, 2025
- 18.4. Benchmarking Analysis, 2025
- 18.5. Aerowent
- 18.6. Atas International, Inc.
- 18.7. C.A.P. Industries, Inc.
- 18.8. Ceco Products
- 18.9. Construction Metals, Inc.
- 18.10. Duracool Roofing
- 18.11. Greenheck Fan Corporation
- 18.12. Kee Lox Manufacturing Co., Inc.
- 18.13. Malta Dynamics
- 18.14. McKenney’s, Inc.
- 18.15. Mitec-America, Inc.
- 18.16. Moffitt Corporation
- 18.17. NCI Group, Inc.
- 18.18. Quarrix Building Products
- 18.19. Roof Products, Inc.
- 18.20. Stinger Worldwide
- 18.21. VENTIL-AIRE
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