Medical Polymer Market by Polymer Type (Acrylics, Acrylonitrile Butadiene Styrene, Biodegradable Polymers), Manufacturing Process (Compression Molding, Extrusion Tubing, Injection Molding), Raw Material, Application - Global Forecast 2025-2032
Description
The Medical Polymer Market was valued at USD 43.13 billion in 2024 and is projected to grow to USD 46.26 billion in 2025, with a CAGR of 7.71%, reaching USD 78.14 billion by 2032.
Setting the Stage for Medical Polymer Innovations that Transform Healthcare Applications Amid Evolving Regulatory Frameworks and Industry Dynamics
Medical polymers are increasingly at the forefront of healthcare innovation, serving as the foundational materials that enable next-generation devices, implants, and diagnostic tools. Their unique combination of biocompatibility, mechanical strength, and manufacturability has positioned these advanced materials as critical enablers of minimally invasive surgery, precision drug delivery, and long-term implant performance. Beyond traditional plastics, the rise of biodegradable and bio-based polymers reflects a growing commitment to sustainability and patient safety, while advanced polycarbonate and polyurethane formulations are offering unprecedented clarity and flexibility for diagnostic applications.
As advancements in additive manufacturing and nanocomposite technology accelerate, medical polymers are becoming more customizable and functionally diverse. This evolution is driven by a convergence of healthcare demands-aging populations, cost containment pressures, and the push for point-of-care solutions-and by regulatory bodies prioritizing material safety and traceability. Consequently, an intricate landscape of technological development, compliance requirements, and clinical validation emerges, requiring stakeholders to navigate both opportunities and complexities as they bring novel polymer solutions from concept to clinic.
Identifying Pivotal Transformative Shifts in the Medical Polymer Landscape Fueled by Technological Breakthroughs and Collaborative Ecosystems
The landscape of medical polymer materials is undergoing transformative shifts propelled by several key drivers. Foremost among these is the integration of digital design and advanced 3D printing techniques, which are enabling patient-specific implants, surgical guides, and biocompatible scaffolds with unprecedented precision. This democratization of custom manufacturing is reshaping traditional supply chains and reducing time-to-market for specialized devices. Concurrently, biobased polymer formulations are emerging from the research pipeline, reflecting both market demand for sustainable solutions and regulatory encouragement of green chemistry principles.
Moreover, cross-sector collaboration between polymer scientists, medical device engineers, and healthcare providers is fostering an ecosystem that propels rapid prototyping, accelerated clinical testing, and iterative design improvements. In parallel, digital twins and simulation platforms are streamlining material qualification processes, helping companies reduce development costs and meet stringent safety standards. Transitioning from commodity plastics to high-performance engineered resins, the industry is embracing a modular approach to material design that anticipates clinical requirements, enhances patient outcomes, and positions companies for agile responses to evolving healthcare needs.
Assessing the Multifaceted Impact of United States Tariffs in 2025 on the Medical Polymer Supply Chain and Competitive Dynamics
In 2025, the enactment of new United States tariffs on select polymer categories has introduced significant complexities for medical device manufacturers and raw material suppliers alike. Heightened import duties on certain high-performance resins have elevated input costs, compelling organizations to reevaluate sourcing strategies and negotiate new long-term supply agreements. Consequently, some manufacturers have opted to localize production, forming strategic joint ventures with domestic chemical producers to mitigate tariff exposure and ensure continuity of supply for critical medical applications.
Beyond cost implications, the tariff landscape has triggered a reassessment of product portfolios, with companies prioritizing high-value, low-volume segments where margin resilience is stronger. This recalibration has led to the consolidation of manufacturing footprints, the adoption of leaner inventory practices, and an intensified focus on alternative resin chemistries not subject to new duties. As a result, industry participants are pressing for enhanced transparency in supplier cost structures and exploring collaborative cost-sharing models to sustain innovation pipelines despite elevated trade barriers.
Extracting Key Segmentation Insights to Illuminate Diverse Polymer Types, Manufacturing Processes, Raw Materials, and Application Domains
The medical polymer market exhibits considerable diversity across material types, manufacturing techniques, feedstocks, and end-use applications, each presenting distinct opportunities and challenges. A closer look at polymer classifications reveals a spectrum from acrylics and acrylonitrile butadiene styrene to polycarbonate, polyethylene terephthalate, polypropylene, polystyrene, and thermoplastic elastomers, along with a growing portfolio of biodegradable resins designed for temporary implants or resorbable scaffolds. Each of these polymers brings unique properties, whether optical clarity for diagnostic devices or tensile strength for load-bearing implantable constructs.
Manufacturing processes further differentiate the market landscape. Injection molding remains indispensable for high-volume disposables and intricate device housings, whereas compression molding and extrusion tubing are pivotal for catheters, fluid delivery components, and patient-centric dressings. Raw material sourcing splits between petrochemical and bio-based origins, with the latter gaining traction in response to sustainability mandates and life-cycle assessment requirements. In application spaces, dental care spans orthodontics and prosthetics; medical devices incorporate diagnostics platforms, single-use disposables, and sophisticated implantable devices; packaging embraces blister packaging and vials & containers; and tissue engineering capitalizes on porous, biocompatible scaffolds. By examining these intersecting dimensions, stakeholders can pinpoint high-growth niches and tailor product development to precise clinical or operational needs.
Unearthing Critical Regional Insights to Highlight Unique Market Drivers across the Americas, Europe Middle East Africa, and Asia-Pacific
Regional dynamics shape the medical polymer market in distinct ways, driven by regulatory frameworks, healthcare infrastructure maturity, and innovation ecosystems. In the Americas, the United States leads with robust R&D investment, regulatory clarity, and an integrated value chain spanning polymer producers, medical device firms, and clinical research organizations. Meanwhile, Latin American markets present expanding opportunities as governments increase healthcare spending and seek cost-effective polymer solutions for widespread vaccination programs and disposable diagnostics.
Across Europe, the Middle East, and Africa, compliance with stringent chemical safety regulations, such as the EU’s REACH framework, drives emphasis on material traceability and life-cycle assessments. Simultaneously, unmapped demand in the Middle East and North Africa is beginning to spur local manufacturing initiatives and strategic partnerships with European innovators. In the Asia-Pacific region, rapid growth in healthcare infrastructure, combined with competitive manufacturing cost structures, fuels the rise of domestic polymer firms and contract manufacturers. As a result, multinational players are forming joint ventures, licensing technologies, and tailoring portfolios to address the unique mix of urban and rural healthcare requirements throughout the region.
Revealing Key Company Insights to Showcase Strategies, Partnerships, and Innovation Pathways Shaping the Medical Polymer Market
A handful of leading companies are steering the direction of medical polymer innovation, leveraging global scale and specialized expertise to drive product development and expand market reach. Major chemical conglomerates are investing heavily in R&D centers dedicated to biocompatible polymer chemistries and sustainable resin production techniques. Simultaneously, niche players are carving out value propositions around high-precision manufacturing, clean-room molding capabilities, and accelerated regulatory submissions by virtue of deep application know-how.
Partnerships and strategic alliances are reshaping competitive positioning, as polymer suppliers collaborate with medical device original equipment manufacturers to co-develop next-generation materials. In parallel, an uptick in mergers and acquisitions reflects the strategic imperative to integrate downstream capabilities, secure supply chain resilience, and access emerging markets. Companies that blend strong intellectual property portfolios with demonstrated clinical validation pathways are gaining a decisive edge, while those with agile commercialization frameworks are achieving faster adoption across surgical, diagnostic, and regenerative medicine segments.
Delivering Actionable Recommendations for Industry Leaders to Navigate Disruption, Optimize Operations, and Leverage Emerging Opportunities
To thrive amid evolving regulatory, trade, and technological landscapes, industry leaders must adopt a proactive, integrated approach. First, diversifying the supplier base to include both established petrochemical producers and emerging bio-based material innovators can hedge against tariff volatility and sustainability mandates. Equally important is investing in digital manufacturing platforms that support rapid prototyping, iterative design optimization, and decentralized production closer to end-user markets.
Moreover, strengthening engagement with regulatory authorities through early collaboration and adaptive compliance strategies will streamline approvals for novel polymer formulations. Organizations should also pursue cross-industry partnerships that combine polymer science expertise with clinical and engineering capabilities, accelerating the path from material innovation to patient impact. Finally, embedding robust life-cycle assessment tools can provide decision-makers with transparency into environmental footprints, aligning product portfolios with evolving procurement standards and stakeholder expectations.
Demystifying the Research Methodology Underpinning Rigorous Data Collection and Analysis Supporting the Medical Polymer Market Findings
This research integrates both primary and secondary data sources to present a rigorous analysis of the medical polymer market. Primary inputs were gathered through structured interviews with polymer scientists, regulatory experts, procurement leaders, and device engineers, offering on-the-ground perspectives on material performance, supply chain resilience, and application trends. These insights were complemented by secondary research, including peer-reviewed journals, industry association publications, patent databases, and regulatory submissions, ensuring a comprehensive foundation of facts and figures.
Data triangulation techniques were applied to validate findings across multiple sources, enhancing the reliability of segmentation breakdowns, tariff impact assessments, and company strategy analyses. Qualitative feedback was coded and synthesized to highlight recurring themes, while quantitative inputs underwent statistical validation to confirm consistency. Finally, all insights were reviewed by an internal advisory board of polymers and healthcare experts to ensure methodological integrity and actionable relevance for market participants.
Concluding Reflections on the Future Trajectory of Medical Polymers Emphasizing Strategic Imperatives and Collaborative Potential
In conclusion, the medical polymer sector stands at a pivotal juncture where material innovation, regulatory evolution, and shifting trade dynamics converge to redefine industry boundaries. Stakeholders who embrace sustainable resin technologies, digital manufacturing, and strategic collaborations will unlock new pathways for device performance and operational efficiency. Tariff-driven supply chain realignments underscore the need for agile sourcing strategies and transparent cost models, while regional market nuances demand tailored approaches that account for regulatory landscapes and infrastructure maturity.
Ultimately, success in this dynamic environment hinges on a balanced pursuit of innovation, compliance, and resilience. By integrating advanced polymer formulations with robust manufacturing platforms and proactive regulatory engagement, organizations can deliver medical solutions that enhance patient outcomes and drive long-term value creation. The next chapter in medical polymer development will be written by those who combine scientific rigor with strategic foresight and collaborative execution.
Please Note: PDF & Excel + Online Access - 1 Year
Setting the Stage for Medical Polymer Innovations that Transform Healthcare Applications Amid Evolving Regulatory Frameworks and Industry Dynamics
Medical polymers are increasingly at the forefront of healthcare innovation, serving as the foundational materials that enable next-generation devices, implants, and diagnostic tools. Their unique combination of biocompatibility, mechanical strength, and manufacturability has positioned these advanced materials as critical enablers of minimally invasive surgery, precision drug delivery, and long-term implant performance. Beyond traditional plastics, the rise of biodegradable and bio-based polymers reflects a growing commitment to sustainability and patient safety, while advanced polycarbonate and polyurethane formulations are offering unprecedented clarity and flexibility for diagnostic applications.
As advancements in additive manufacturing and nanocomposite technology accelerate, medical polymers are becoming more customizable and functionally diverse. This evolution is driven by a convergence of healthcare demands-aging populations, cost containment pressures, and the push for point-of-care solutions-and by regulatory bodies prioritizing material safety and traceability. Consequently, an intricate landscape of technological development, compliance requirements, and clinical validation emerges, requiring stakeholders to navigate both opportunities and complexities as they bring novel polymer solutions from concept to clinic.
Identifying Pivotal Transformative Shifts in the Medical Polymer Landscape Fueled by Technological Breakthroughs and Collaborative Ecosystems
The landscape of medical polymer materials is undergoing transformative shifts propelled by several key drivers. Foremost among these is the integration of digital design and advanced 3D printing techniques, which are enabling patient-specific implants, surgical guides, and biocompatible scaffolds with unprecedented precision. This democratization of custom manufacturing is reshaping traditional supply chains and reducing time-to-market for specialized devices. Concurrently, biobased polymer formulations are emerging from the research pipeline, reflecting both market demand for sustainable solutions and regulatory encouragement of green chemistry principles.
Moreover, cross-sector collaboration between polymer scientists, medical device engineers, and healthcare providers is fostering an ecosystem that propels rapid prototyping, accelerated clinical testing, and iterative design improvements. In parallel, digital twins and simulation platforms are streamlining material qualification processes, helping companies reduce development costs and meet stringent safety standards. Transitioning from commodity plastics to high-performance engineered resins, the industry is embracing a modular approach to material design that anticipates clinical requirements, enhances patient outcomes, and positions companies for agile responses to evolving healthcare needs.
Assessing the Multifaceted Impact of United States Tariffs in 2025 on the Medical Polymer Supply Chain and Competitive Dynamics
In 2025, the enactment of new United States tariffs on select polymer categories has introduced significant complexities for medical device manufacturers and raw material suppliers alike. Heightened import duties on certain high-performance resins have elevated input costs, compelling organizations to reevaluate sourcing strategies and negotiate new long-term supply agreements. Consequently, some manufacturers have opted to localize production, forming strategic joint ventures with domestic chemical producers to mitigate tariff exposure and ensure continuity of supply for critical medical applications.
Beyond cost implications, the tariff landscape has triggered a reassessment of product portfolios, with companies prioritizing high-value, low-volume segments where margin resilience is stronger. This recalibration has led to the consolidation of manufacturing footprints, the adoption of leaner inventory practices, and an intensified focus on alternative resin chemistries not subject to new duties. As a result, industry participants are pressing for enhanced transparency in supplier cost structures and exploring collaborative cost-sharing models to sustain innovation pipelines despite elevated trade barriers.
Extracting Key Segmentation Insights to Illuminate Diverse Polymer Types, Manufacturing Processes, Raw Materials, and Application Domains
The medical polymer market exhibits considerable diversity across material types, manufacturing techniques, feedstocks, and end-use applications, each presenting distinct opportunities and challenges. A closer look at polymer classifications reveals a spectrum from acrylics and acrylonitrile butadiene styrene to polycarbonate, polyethylene terephthalate, polypropylene, polystyrene, and thermoplastic elastomers, along with a growing portfolio of biodegradable resins designed for temporary implants or resorbable scaffolds. Each of these polymers brings unique properties, whether optical clarity for diagnostic devices or tensile strength for load-bearing implantable constructs.
Manufacturing processes further differentiate the market landscape. Injection molding remains indispensable for high-volume disposables and intricate device housings, whereas compression molding and extrusion tubing are pivotal for catheters, fluid delivery components, and patient-centric dressings. Raw material sourcing splits between petrochemical and bio-based origins, with the latter gaining traction in response to sustainability mandates and life-cycle assessment requirements. In application spaces, dental care spans orthodontics and prosthetics; medical devices incorporate diagnostics platforms, single-use disposables, and sophisticated implantable devices; packaging embraces blister packaging and vials & containers; and tissue engineering capitalizes on porous, biocompatible scaffolds. By examining these intersecting dimensions, stakeholders can pinpoint high-growth niches and tailor product development to precise clinical or operational needs.
Unearthing Critical Regional Insights to Highlight Unique Market Drivers across the Americas, Europe Middle East Africa, and Asia-Pacific
Regional dynamics shape the medical polymer market in distinct ways, driven by regulatory frameworks, healthcare infrastructure maturity, and innovation ecosystems. In the Americas, the United States leads with robust R&D investment, regulatory clarity, and an integrated value chain spanning polymer producers, medical device firms, and clinical research organizations. Meanwhile, Latin American markets present expanding opportunities as governments increase healthcare spending and seek cost-effective polymer solutions for widespread vaccination programs and disposable diagnostics.
Across Europe, the Middle East, and Africa, compliance with stringent chemical safety regulations, such as the EU’s REACH framework, drives emphasis on material traceability and life-cycle assessments. Simultaneously, unmapped demand in the Middle East and North Africa is beginning to spur local manufacturing initiatives and strategic partnerships with European innovators. In the Asia-Pacific region, rapid growth in healthcare infrastructure, combined with competitive manufacturing cost structures, fuels the rise of domestic polymer firms and contract manufacturers. As a result, multinational players are forming joint ventures, licensing technologies, and tailoring portfolios to address the unique mix of urban and rural healthcare requirements throughout the region.
Revealing Key Company Insights to Showcase Strategies, Partnerships, and Innovation Pathways Shaping the Medical Polymer Market
A handful of leading companies are steering the direction of medical polymer innovation, leveraging global scale and specialized expertise to drive product development and expand market reach. Major chemical conglomerates are investing heavily in R&D centers dedicated to biocompatible polymer chemistries and sustainable resin production techniques. Simultaneously, niche players are carving out value propositions around high-precision manufacturing, clean-room molding capabilities, and accelerated regulatory submissions by virtue of deep application know-how.
Partnerships and strategic alliances are reshaping competitive positioning, as polymer suppliers collaborate with medical device original equipment manufacturers to co-develop next-generation materials. In parallel, an uptick in mergers and acquisitions reflects the strategic imperative to integrate downstream capabilities, secure supply chain resilience, and access emerging markets. Companies that blend strong intellectual property portfolios with demonstrated clinical validation pathways are gaining a decisive edge, while those with agile commercialization frameworks are achieving faster adoption across surgical, diagnostic, and regenerative medicine segments.
Delivering Actionable Recommendations for Industry Leaders to Navigate Disruption, Optimize Operations, and Leverage Emerging Opportunities
To thrive amid evolving regulatory, trade, and technological landscapes, industry leaders must adopt a proactive, integrated approach. First, diversifying the supplier base to include both established petrochemical producers and emerging bio-based material innovators can hedge against tariff volatility and sustainability mandates. Equally important is investing in digital manufacturing platforms that support rapid prototyping, iterative design optimization, and decentralized production closer to end-user markets.
Moreover, strengthening engagement with regulatory authorities through early collaboration and adaptive compliance strategies will streamline approvals for novel polymer formulations. Organizations should also pursue cross-industry partnerships that combine polymer science expertise with clinical and engineering capabilities, accelerating the path from material innovation to patient impact. Finally, embedding robust life-cycle assessment tools can provide decision-makers with transparency into environmental footprints, aligning product portfolios with evolving procurement standards and stakeholder expectations.
Demystifying the Research Methodology Underpinning Rigorous Data Collection and Analysis Supporting the Medical Polymer Market Findings
This research integrates both primary and secondary data sources to present a rigorous analysis of the medical polymer market. Primary inputs were gathered through structured interviews with polymer scientists, regulatory experts, procurement leaders, and device engineers, offering on-the-ground perspectives on material performance, supply chain resilience, and application trends. These insights were complemented by secondary research, including peer-reviewed journals, industry association publications, patent databases, and regulatory submissions, ensuring a comprehensive foundation of facts and figures.
Data triangulation techniques were applied to validate findings across multiple sources, enhancing the reliability of segmentation breakdowns, tariff impact assessments, and company strategy analyses. Qualitative feedback was coded and synthesized to highlight recurring themes, while quantitative inputs underwent statistical validation to confirm consistency. Finally, all insights were reviewed by an internal advisory board of polymers and healthcare experts to ensure methodological integrity and actionable relevance for market participants.
Concluding Reflections on the Future Trajectory of Medical Polymers Emphasizing Strategic Imperatives and Collaborative Potential
In conclusion, the medical polymer sector stands at a pivotal juncture where material innovation, regulatory evolution, and shifting trade dynamics converge to redefine industry boundaries. Stakeholders who embrace sustainable resin technologies, digital manufacturing, and strategic collaborations will unlock new pathways for device performance and operational efficiency. Tariff-driven supply chain realignments underscore the need for agile sourcing strategies and transparent cost models, while regional market nuances demand tailored approaches that account for regulatory landscapes and infrastructure maturity.
Ultimately, success in this dynamic environment hinges on a balanced pursuit of innovation, compliance, and resilience. By integrating advanced polymer formulations with robust manufacturing platforms and proactive regulatory engagement, organizations can deliver medical solutions that enhance patient outcomes and drive long-term value creation. The next chapter in medical polymer development will be written by those who combine scientific rigor with strategic foresight and collaborative execution.
Please Note: PDF & Excel + Online Access - 1 Year
Table of Contents
181 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. Accelerated adoption of bioresorbable polymer scaffolds in cardiovascular interventions
- 5.2. Integration of antimicrobial polymer coatings in surgical instruments to reduce infection rates
- 5.3. Expansion of 3D printed medical devices using photopolymer resins with enhanced biocompatibility
- 5.4. Development of stimuli responsive polymer drug delivery systems for targeted cancer therapies
- 5.5. Growing utilization of silicone elastomers in wearable biosensors for continuous patient monitoring
- 5.6. Advancements in polymer based hemostatic dressings for rapid wound closure and bleeding control
- 5.7. Emergence of polymer hydrogels enabling 3D cell culture and tissue engineering applications in vitro
- 5.8. Regulatory approval challenges for novel polymeric medical implants driving design optimization strategies
- 5.9. Implementation of sustainable bio based polymers to reduce environmental impact in medical packaging
- 5.10. Innovations in copolymer blends enhancing mechanical strength of load bearing orthopedic implants
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Medical Polymer Market, by Polymer Type
- 8.1. Acrylics
- 8.2. Acrylonitrile Butadiene Styrene
- 8.3. Biodegradable Polymers
- 8.4. Polycarbonate
- 8.5. Polyethylene
- 8.6. Polyethylene Terephthalate
- 8.7. Polypropylene
- 8.8. Polystyrene
- 8.9. Polyvinyl Chloride
- 8.10. Thermoplastic Elastomers
- 9. Medical Polymer Market, by Manufacturing Process
- 9.1. Compression Molding
- 9.2. Extrusion Tubing
- 9.3. Injection Molding
- 10. Medical Polymer Market, by Raw Material
- 10.1. Bio-Based
- 10.2. Petrochemical
- 11. Medical Polymer Market, by Application
- 11.1. Dental Care
- 11.1.1. Orthodontics
- 11.1.2. Prosthetics
- 11.2. Medical Devices
- 11.2.1. Diagnostics
- 11.2.2. Disposables
- 11.2.3. Implantable Devices
- 11.3. Packaging
- 11.3.1. Blister Packaging
- 11.3.2. Vials & Containers
- 11.4. Tissue Engineering
- 12. Medical Polymer 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. Medical Polymer Market, by Group
- 13.1. ASEAN
- 13.2. GCC
- 13.3. European Union
- 13.4. BRICS
- 13.5. G7
- 13.6. NATO
- 14. Medical Polymer 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. Arkema Group
- 15.3.2. Avient Corporation by PolyOne Corporation
- 15.3.3. BASF SE
- 15.3.4. Biesterfeld AG
- 15.3.5. Celanese Corporation
- 15.3.6. Corbion NV
- 15.3.7. Covestro AG
- 15.3.8. DSM-Firmenich AG
- 15.3.9. DuPont de Nemours, Inc.
- 15.3.10. Eastman Chemical Company
- 15.3.11. Evonik Industries AG
- 15.3.12. Exxon Mobil Corporation
- 15.3.13. GELITA AG
- 15.3.14. Green Dot Bioplastics Inc.
- 15.3.15. Huizhou Foryou Medical Devices Co., Ltd.
- 15.3.16. Invibio Ltd. by Victrex PLC
- 15.3.17. ITV Denkendorf Product Service GmbH
- 15.3.18. KRATON CORPORATION by KRATON CORPORATION
- 15.3.19. Lubrizol Corporation
- 15.3.20. Merck KGaA
- 15.3.21. NatureWorks LLC by Cargill Inc.
- 15.3.22. Rodenburg Biopolymers
- 15.3.23. Solvay SA
- 15.3.24. Thermo Fisher Scientific Inc.
- 15.3.25. Toray Industries, Inc.
- 15.3.26. Zeus Company LLC
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