Biomaterials Market by Type (Ceramics, Metallic, Natural), Classification (Bioactive Materials, Biocompatible Materials, Bioinert Materials), End User, Application - Global Forecast 2025-2032
Description
The Biomaterials Market was valued at USD 49.94 billion in 2024 and is projected to grow to USD 56.07 billion in 2025, with a CAGR of 12.84%, reaching USD 131.30 billion by 2032.
Foundational Insights Shaping the Future of Biomaterials Through Pioneering Research and Dynamic Cross-Sector Collaborations
The biomaterials market stands at a pivotal juncture where scientific breakthroughs and cross-functional partnerships are setting the stage for unprecedented advancements. As life sciences converge with engineering disciplines, novel materials inspired by nature are being engineered to address unmet clinical needs, offering architects of medical innovation the tools to redefine patient care. At the core of this evolution are collaborative ecosystems in which academia, specialized research centers, and leading industry players coalesce around shared objectives, accelerating the translation of laboratory discoveries into marketable solutions.
In this transformative environment, robust research and development frameworks are underpinning the creation of next-generation implants, drug delivery systems, and regenerative scaffolds. Continuous investment in advanced characterization techniques and biocompatibility testing is pushing the boundaries of what biomaterials can achieve. Moreover, as regulatory pathways become increasingly sophisticated, stakeholders are aligning early on to navigate complex approval processes, ensuring that emerging materials meet stringent safety and efficacy standards. This introduction lays the groundwork for a deeper exploration of the forces reshaping materials science, illuminating the strategic pathways that organizations must follow to lead in an era defined by rapid innovation and collaborative prowess
Revolutionary Shifts Driving Disruption in Biomaterials Markets with Converging Technologies and Evolving Regulatory Landscapes
The biomaterials landscape is undergoing a profound metamorphosis driven by the convergence of additive manufacturing, artificial intelligence, and precision medicine paradigms. Innovations in three-dimensional printing techniques are enabling the creation of patient-specific implants with complex architectures, while machine learning algorithms are optimizing material formulations for enhanced performance. These technological inflection points are not occurring in isolation; rather, they are being amplified by an increasingly interconnected ecosystem of forward-thinking enterprises, research institutions, and healthcare providers.
Concurrently, regulatory environments across major markets are evolving to address the unique challenges posed by these advanced materials. The introduction of more rigorous post-market surveillance requirements and the harmonization of international standards are urging developers to adopt quality-by-design principles early in the product lifecycle. Sustainability considerations are further shaping material selection and process innovation, prompting an industry-wide movement toward greener chemistries and biodegradable solutions. Together, these shifts are redefining competitive dynamics, requiring stakeholders to adapt their R&D strategies, forge strategic alliances, and anticipate emerging compliance frameworks in order to capture the full potential of this new era
Assessing the Multifaceted Consequences of United States Tariffs on Biomaterials Supply Chains Regulatory Compliance and Cost Structures in 2025
The imposition of tariffs on biomaterial imports into the United States has introduced a complex layer of financial and operational challenges for supply chain managers and product developers alike. Raw materials sourced from global suppliers are now subject to additional levies, elevating input costs and creating pressure points that reverberate across manufacturing timelines. In response, many organizations have initiated dual-sourcing strategies, reallocating production to domestic or near-shore partners to mitigate exposure to fluctuating tariff schedules and minimize potential supply disruptions.
Beyond immediate cost impacts, these trade policy measures are reshaping global collaboration models. Companies are reevaluating licensing agreements, technology transfers, and joint development programs to ensure that intellectual property remains protected and cost-effective under revised import frameworks. Furthermore, research partnerships are adapting to prioritize locally available feedstocks and alternative synthesis routes, fostering a stronger emphasis on circular economy principles. By understanding these cumulative effects, decision makers can proactively restructure procurement practices, optimize inventory management, and refine pricing strategies to maintain competitive positioning in the face of an increasingly complex regulatory environment
Unveiling Critical Segmentation Perspectives Highlighting Type Classification End User Application and Advanced Polymer and Ceramic Variants
An in-depth segmentation analysis reveals the nuanced interplay of material categories and their subtypes that drive competitive differentiation. On the basis of type, the biomaterials domain encompasses ceramics, metallic substances, natural compounds, and a spectrum of synthetic polymers ranging from polycaprolactone and polyglycolic acid to polylactic acid, polylactic-co-glycolic acid, polyethylene, polypropylene, polyurethane, and polyvinyl alcohol. Within ceramics, further diversification is apparent through aluminum oxide variants, bioglass formulations, hydroxyapatite composites, and zirconia-based scaffolds, each offering distinct bioactivity profiles and mechanical properties.
When classified by biological interaction, materials can be categorized as bioactive, biocompatible, or bioinert, reflecting their capacity to engage with physiological environments. This axis of classification directly influences applications spanning cardiovascular guidewires and vascular grafts, dental bone grafts and tissue regeneration membranes, ophthalmology implants, orthopedic joint replacements and spine devices, urinary stents, and wound healing products such as adhesion barriers, internal tissue sealants, skin substitutes, and surgical hemostats. End-user segmentation further underscores the market’s complexity, with biotechnology firms, hospitals, research laboratories, and specialty clinics each exerting unique requirements on material selection, regulatory pathways, and performance validation
Interpreting Regional Dynamics Shaping Growth Trajectories Across the Americas Europe Middle East and Africa and Asia Pacific Arenas
Regional dynamics play a decisive role in shaping the trajectory of biomaterials innovation and adoption across key geographies. In the Americas, well-established regulatory frameworks, coupled with robust funding mechanisms, have fostered a fertile environment for translational research and commercialization. Industrial clusters in the United States and Canada are leveraging proximity to premier academic institutions, enabling agile collaboration and acceleration of proof-of-concept studies.
Across Europe, the Middle East and Africa, diverse regulatory regimes are converging around unified standards, stimulating cross-border partnerships and harmonized market entry strategies. Investment in next-generation manufacturing facilities is on the rise, as stakeholders pursue both high-value specialty materials and scalable production platforms. Meanwhile, in the Asia Pacific region, rapid growth in healthcare infrastructure and an expanding base of domestic manufacturers are driving heightened demand for cost-effective biomaterials solutions. Governments and private investors are channeling resources into greenfield facilities and collaborative research consortia, catalyzing innovation and strengthening supply chain resilience
Exploring the Strategic Imperatives and Innovation Roadmaps of Leading Biomaterials Companies Driving Competitive Advantage
Leading players in the biomaterials sector are distinguishing themselves through strategic investment in research platforms, targeted acquisitions, and the formation of consortia to unlock new therapeutic possibilities. Global medical device and implant manufacturers are enhancing their product portfolios by integrating advanced polymer formulations and ceramic composites, while specialty chemical providers are forging partnerships to optimize functionalization processes and surface treatments. At the same time, emerging innovators are leveraging modular design approaches, enabling rapid customization for specific patient demographics and surgical techniques.
Competitive positioning is further influenced by clinical trial activities, intellectual property strategies, and participation in standards-setting bodies. Organizations that prioritize transparency in biocompatibility testing and post-market performance tracking are gaining trust among regulators and end users, accelerating adoption cycles. Meanwhile, the pursuit of sustainable manufacturing practices is fostering collaborations between materials scientists and environmental experts, driving the development of recyclable and biodegradable solutions that address both clinical efficacy and ecological responsibility
Actionable Roadmap and Strategic Guidelines for Industry Leaders to Navigate Disruption Embrace Innovation and Capitalize on Emerging Biomaterials Opportunities
Industry leaders aiming to capture emerging opportunities must align their strategic roadmaps with the acceleration of personalized medicine trends and sustainability imperatives. To this end, prioritizing investment in advanced polymer chemistries and hybrid material systems will enable the creation of next-generation implants with tunable degradation rates and enhanced mechanical resilience. In parallel, establishing partnerships with academic centers and specialized test facilities can streamline validation workflows and reduce time-to-market.
Additionally, diversification of procurement strategies by developing regional supply hubs and exploring alternative feedstocks will mitigate exposure to trade policy uncertainties. Embracing digital twin technologies and predictive analytics can further optimize manufacturing processes, ensuring consistent quality across production batches. By integrating these actionable guidelines into their operational blueprint, decision makers can navigate disruption with agility, secure sustainable competitive advantages, and position their organizations to lead the evolution of the biomaterials landscape
Robust Research Methodology Detailing Data Collection Analytical Framework and Validation Techniques Underpinning the Biomaterials Market Study
This report’s findings are underpinned by a rigorous methodology combining primary and secondary research, designed to capture a comprehensive view of the biomaterials ecosystem. Secondary sources including scientific journals, regulatory filings, and patent databases provided a foundational understanding of material properties, clinical applications, and emerging trends. This was complemented by primary interviews with key opinion leaders, supply chain executives, regulatory experts, and end-user practitioners, ensuring that quantitative data is contextualized by real-world insights.
Data triangulation techniques were employed to validate information across multiple channels, while an analytical framework integrating Porter’s Five Forces and technology readiness assessments enabled thorough competitive and innovation landscape mapping. Statistical analyses were conducted to identify performance drivers and potential bottlenecks, and a multi-stage validation process ensured that assumptions align with the most current market realities. This robust methodological approach delivers confidence in the credibility and relevance of the insights presented, supporting informed decision making
Synthesizing Key Findings and Strategic Perspectives to Conclude the Comprehensive Exploration of Global Biomaterials Trends
As this study attests, the biomaterials sector stands at the intersection of transformative technologies, evolving regulatory landscapes, and shifting global trade dynamics. The interplay between advanced material science, digital innovation, and strategic collaboration is generating a rich tapestry of opportunities for those prepared to embrace complexity. From the diversification of segmentation strategies to the optimization of regional footprints and the refinement of sourcing models, each insight underscores the need for a holistic approach to market leadership.
Looking ahead, organizations that deftly integrate sustainable practices with agile innovation frameworks will be best positioned to deliver differentiated solutions and secure a competitive edge. By harnessing the detailed findings and strategic perspectives offered here, decision makers can chart a clear path through the challenges of tariffs, compliance shifts, and supply chain constraints. In doing so, they will unlock the full potential of biomaterials to redefine patient outcomes and catalyze the next wave of medical breakthroughs
Please Note: PDF & Excel + Online Access - 1 Year
Foundational Insights Shaping the Future of Biomaterials Through Pioneering Research and Dynamic Cross-Sector Collaborations
The biomaterials market stands at a pivotal juncture where scientific breakthroughs and cross-functional partnerships are setting the stage for unprecedented advancements. As life sciences converge with engineering disciplines, novel materials inspired by nature are being engineered to address unmet clinical needs, offering architects of medical innovation the tools to redefine patient care. At the core of this evolution are collaborative ecosystems in which academia, specialized research centers, and leading industry players coalesce around shared objectives, accelerating the translation of laboratory discoveries into marketable solutions.
In this transformative environment, robust research and development frameworks are underpinning the creation of next-generation implants, drug delivery systems, and regenerative scaffolds. Continuous investment in advanced characterization techniques and biocompatibility testing is pushing the boundaries of what biomaterials can achieve. Moreover, as regulatory pathways become increasingly sophisticated, stakeholders are aligning early on to navigate complex approval processes, ensuring that emerging materials meet stringent safety and efficacy standards. This introduction lays the groundwork for a deeper exploration of the forces reshaping materials science, illuminating the strategic pathways that organizations must follow to lead in an era defined by rapid innovation and collaborative prowess
Revolutionary Shifts Driving Disruption in Biomaterials Markets with Converging Technologies and Evolving Regulatory Landscapes
The biomaterials landscape is undergoing a profound metamorphosis driven by the convergence of additive manufacturing, artificial intelligence, and precision medicine paradigms. Innovations in three-dimensional printing techniques are enabling the creation of patient-specific implants with complex architectures, while machine learning algorithms are optimizing material formulations for enhanced performance. These technological inflection points are not occurring in isolation; rather, they are being amplified by an increasingly interconnected ecosystem of forward-thinking enterprises, research institutions, and healthcare providers.
Concurrently, regulatory environments across major markets are evolving to address the unique challenges posed by these advanced materials. The introduction of more rigorous post-market surveillance requirements and the harmonization of international standards are urging developers to adopt quality-by-design principles early in the product lifecycle. Sustainability considerations are further shaping material selection and process innovation, prompting an industry-wide movement toward greener chemistries and biodegradable solutions. Together, these shifts are redefining competitive dynamics, requiring stakeholders to adapt their R&D strategies, forge strategic alliances, and anticipate emerging compliance frameworks in order to capture the full potential of this new era
Assessing the Multifaceted Consequences of United States Tariffs on Biomaterials Supply Chains Regulatory Compliance and Cost Structures in 2025
The imposition of tariffs on biomaterial imports into the United States has introduced a complex layer of financial and operational challenges for supply chain managers and product developers alike. Raw materials sourced from global suppliers are now subject to additional levies, elevating input costs and creating pressure points that reverberate across manufacturing timelines. In response, many organizations have initiated dual-sourcing strategies, reallocating production to domestic or near-shore partners to mitigate exposure to fluctuating tariff schedules and minimize potential supply disruptions.
Beyond immediate cost impacts, these trade policy measures are reshaping global collaboration models. Companies are reevaluating licensing agreements, technology transfers, and joint development programs to ensure that intellectual property remains protected and cost-effective under revised import frameworks. Furthermore, research partnerships are adapting to prioritize locally available feedstocks and alternative synthesis routes, fostering a stronger emphasis on circular economy principles. By understanding these cumulative effects, decision makers can proactively restructure procurement practices, optimize inventory management, and refine pricing strategies to maintain competitive positioning in the face of an increasingly complex regulatory environment
Unveiling Critical Segmentation Perspectives Highlighting Type Classification End User Application and Advanced Polymer and Ceramic Variants
An in-depth segmentation analysis reveals the nuanced interplay of material categories and their subtypes that drive competitive differentiation. On the basis of type, the biomaterials domain encompasses ceramics, metallic substances, natural compounds, and a spectrum of synthetic polymers ranging from polycaprolactone and polyglycolic acid to polylactic acid, polylactic-co-glycolic acid, polyethylene, polypropylene, polyurethane, and polyvinyl alcohol. Within ceramics, further diversification is apparent through aluminum oxide variants, bioglass formulations, hydroxyapatite composites, and zirconia-based scaffolds, each offering distinct bioactivity profiles and mechanical properties.
When classified by biological interaction, materials can be categorized as bioactive, biocompatible, or bioinert, reflecting their capacity to engage with physiological environments. This axis of classification directly influences applications spanning cardiovascular guidewires and vascular grafts, dental bone grafts and tissue regeneration membranes, ophthalmology implants, orthopedic joint replacements and spine devices, urinary stents, and wound healing products such as adhesion barriers, internal tissue sealants, skin substitutes, and surgical hemostats. End-user segmentation further underscores the market’s complexity, with biotechnology firms, hospitals, research laboratories, and specialty clinics each exerting unique requirements on material selection, regulatory pathways, and performance validation
Interpreting Regional Dynamics Shaping Growth Trajectories Across the Americas Europe Middle East and Africa and Asia Pacific Arenas
Regional dynamics play a decisive role in shaping the trajectory of biomaterials innovation and adoption across key geographies. In the Americas, well-established regulatory frameworks, coupled with robust funding mechanisms, have fostered a fertile environment for translational research and commercialization. Industrial clusters in the United States and Canada are leveraging proximity to premier academic institutions, enabling agile collaboration and acceleration of proof-of-concept studies.
Across Europe, the Middle East and Africa, diverse regulatory regimes are converging around unified standards, stimulating cross-border partnerships and harmonized market entry strategies. Investment in next-generation manufacturing facilities is on the rise, as stakeholders pursue both high-value specialty materials and scalable production platforms. Meanwhile, in the Asia Pacific region, rapid growth in healthcare infrastructure and an expanding base of domestic manufacturers are driving heightened demand for cost-effective biomaterials solutions. Governments and private investors are channeling resources into greenfield facilities and collaborative research consortia, catalyzing innovation and strengthening supply chain resilience
Exploring the Strategic Imperatives and Innovation Roadmaps of Leading Biomaterials Companies Driving Competitive Advantage
Leading players in the biomaterials sector are distinguishing themselves through strategic investment in research platforms, targeted acquisitions, and the formation of consortia to unlock new therapeutic possibilities. Global medical device and implant manufacturers are enhancing their product portfolios by integrating advanced polymer formulations and ceramic composites, while specialty chemical providers are forging partnerships to optimize functionalization processes and surface treatments. At the same time, emerging innovators are leveraging modular design approaches, enabling rapid customization for specific patient demographics and surgical techniques.
Competitive positioning is further influenced by clinical trial activities, intellectual property strategies, and participation in standards-setting bodies. Organizations that prioritize transparency in biocompatibility testing and post-market performance tracking are gaining trust among regulators and end users, accelerating adoption cycles. Meanwhile, the pursuit of sustainable manufacturing practices is fostering collaborations between materials scientists and environmental experts, driving the development of recyclable and biodegradable solutions that address both clinical efficacy and ecological responsibility
Actionable Roadmap and Strategic Guidelines for Industry Leaders to Navigate Disruption Embrace Innovation and Capitalize on Emerging Biomaterials Opportunities
Industry leaders aiming to capture emerging opportunities must align their strategic roadmaps with the acceleration of personalized medicine trends and sustainability imperatives. To this end, prioritizing investment in advanced polymer chemistries and hybrid material systems will enable the creation of next-generation implants with tunable degradation rates and enhanced mechanical resilience. In parallel, establishing partnerships with academic centers and specialized test facilities can streamline validation workflows and reduce time-to-market.
Additionally, diversification of procurement strategies by developing regional supply hubs and exploring alternative feedstocks will mitigate exposure to trade policy uncertainties. Embracing digital twin technologies and predictive analytics can further optimize manufacturing processes, ensuring consistent quality across production batches. By integrating these actionable guidelines into their operational blueprint, decision makers can navigate disruption with agility, secure sustainable competitive advantages, and position their organizations to lead the evolution of the biomaterials landscape
Robust Research Methodology Detailing Data Collection Analytical Framework and Validation Techniques Underpinning the Biomaterials Market Study
This report’s findings are underpinned by a rigorous methodology combining primary and secondary research, designed to capture a comprehensive view of the biomaterials ecosystem. Secondary sources including scientific journals, regulatory filings, and patent databases provided a foundational understanding of material properties, clinical applications, and emerging trends. This was complemented by primary interviews with key opinion leaders, supply chain executives, regulatory experts, and end-user practitioners, ensuring that quantitative data is contextualized by real-world insights.
Data triangulation techniques were employed to validate information across multiple channels, while an analytical framework integrating Porter’s Five Forces and technology readiness assessments enabled thorough competitive and innovation landscape mapping. Statistical analyses were conducted to identify performance drivers and potential bottlenecks, and a multi-stage validation process ensured that assumptions align with the most current market realities. This robust methodological approach delivers confidence in the credibility and relevance of the insights presented, supporting informed decision making
Synthesizing Key Findings and Strategic Perspectives to Conclude the Comprehensive Exploration of Global Biomaterials Trends
As this study attests, the biomaterials sector stands at the intersection of transformative technologies, evolving regulatory landscapes, and shifting global trade dynamics. The interplay between advanced material science, digital innovation, and strategic collaboration is generating a rich tapestry of opportunities for those prepared to embrace complexity. From the diversification of segmentation strategies to the optimization of regional footprints and the refinement of sourcing models, each insight underscores the need for a holistic approach to market leadership.
Looking ahead, organizations that deftly integrate sustainable practices with agile innovation frameworks will be best positioned to deliver differentiated solutions and secure a competitive edge. By harnessing the detailed findings and strategic perspectives offered here, decision makers can chart a clear path through the challenges of tariffs, compliance shifts, and supply chain constraints. In doing so, they will unlock the full potential of biomaterials to redefine patient outcomes and catalyze the next wave of medical breakthroughs
Please Note: PDF & Excel + Online Access - 1 Year
Table of Contents
186 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. Development of 3D-printed biodegradable scaffolds for tissue regeneration
- 5.2. Adoption of antimicrobial biomaterials to reduce hospital acquired infections
- 5.3. Innovations in hydrogel based delivery systems for targeted cancer therapies
- 5.4. Advancements in smart biomaterials that respond to physiological stimuli
- 5.5. Emergence of sustainable marine derived chitosan biomaterials in wound care
- 5.6. Growth of algae derived polymers as ecofriendly alternatives in medical device coatings
- 5.7. Integration of artificial intelligence in design of next generation biomaterials for personalized medicine
- 5.8. Advances in bioresorbable electronics using conductive polymers for implantable sensors
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Biomaterials Market, by Type
- 8.1. Ceramics
- 8.1.1. Alumina
- 8.1.2. Bioglass
- 8.1.3. Hydroxyapatite
- 8.1.4. Zirconia
- 8.2. Metallic
- 8.3. Natural
- 8.4. Synthetic Polymers
- 8.4.1. PCL (Polycaprolactone)
- 8.4.2. PGA (Polyglycolic acid)
- 8.4.3. PLA (Polylactic acid)
- 8.4.4. PLGA (Polylactic-co-glycolic acid)
- 8.4.5. Polyethylene (PE)
- 8.4.6. Polypropylene (PP)
- 8.4.7. Polyurethane (PU)
- 8.4.8. Polyvinyl alcohol (PVA)
- 9. Biomaterials Market, by Classification
- 9.1. Bioactive Materials
- 9.2. Biocompatible Materials
- 9.3. Bioinert Materials
- 10. Biomaterials Market, by End User
- 10.1. Biotechnology Companies
- 10.2. Hospitals
- 10.3. Research Laboratories
- 10.4. Specialty Clinics
- 11. Biomaterials Market, by Application
- 11.1. Cardiovascular
- 11.1.1. Guidewires
- 11.1.2. Implantable Cardiac Defibrillators
- 11.1.3. Pacemakers
- 11.1.4. Sensors
- 11.1.5. Stents
- 11.1.6. Vascular Grafts
- 11.2. Dental
- 11.2.1. Bone Grafts & Substitutes
- 11.2.2. Dental Implants
- 11.2.3. Dental Membranes
- 11.2.4. Tissue Regeneration Materials
- 11.3. Ophthalmology
- 11.4. Orthopedic
- 11.4.1. Bioresorbable Tissue Fixation Products
- 11.4.2. Joint Replacement biomaterials
- 11.4.3. Orthobiologics
- 11.4.4. Spine Biomaterials
- 11.4.5. Viscosupplementation
- 11.5. Urinary
- 11.6. Wound Healing
- 11.6.1. Adhesion Barrier
- 11.6.2. Fracture Healing Device
- 11.6.3. Internal Tissue Sealant
- 11.6.4. Skin Substitutes
- 11.6.5. Surgical Hemostats
- 12. Biomaterials 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. Biomaterials Market, by Group
- 13.1. ASEAN
- 13.2. GCC
- 13.3. European Union
- 13.4. BRICS
- 13.5. G7
- 13.6. NATO
- 14. Biomaterials 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. Aroa Biosurgery Limited
- 15.3.2. BASF SE
- 15.3.3. Berkeley Advanced Biomaterials Inc.
- 15.3.4. Bezwada Biomedical, LLC
- 15.3.5. Carpenter Technology Corporation
- 15.3.6. Celanese Corporation
- 15.3.7. CoorsTek, Inc.
- 15.3.8. Corbion N.V.
- 15.3.9. Covestro AG
- 15.3.10. Dentsply Sirona Inc.
- 15.3.11. DSM-Firmenich AG
- 15.3.12. Evonik Industries AG
- 15.3.13. Exactech, Inc.
- 15.3.14. Heraeus Holding GmbH
- 15.3.15. Invibio Limited
- 15.3.16. Medtronic plc
- 15.3.17. Modern Meadow, Inc.
- 15.3.18. MycoWorks, Inc.
- 15.3.19. Noble Biomaterials, Inc.
- 15.3.20. Smith & Nephew plc
- 15.3.21. Stryker Corporation
- 15.3.22. TissueForm, Inc.
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