Endoscopy Visualization Systems Market by Product Type (Capsule Endoscope Systems, Flexible Endoscope Systems, Hybrid Endoscope Systems), Application (Ear Nose Throat, Gastroenterology, Gynecology), End User, Modality - Global Forecast 2025-2032
Description
The Endoscopy Visualization Systems Market was valued at USD 23.61 billion in 2024 and is projected to grow to USD 26.41 billion in 2025, with a CAGR of 12.12%, reaching USD 58.99 billion by 2032.
Framing the era of imaging-led procedural care where clinical outcomes, workflow integration, and infection control jointly determine endoscopy system selection
Endoscopy visualization is at the intersection of optics, digital imaging, and clinical workflow optimization, driving demand for solutions that improve diagnostic accuracy and procedural efficiency. Clinicians and procurement leaders are evaluating systems not only for image fidelity and ergonomics but also for integration with electronic health records, AI-assisted analytics, and infection control protocols. As a result, adoption decisions increasingly hinge on a system’s ability to deliver reproducible outcomes across inpatient and outpatient environments while minimizing lifecycle costs and downtime.
Looking ahead, the landscape will be determined by how vendors balance technological sophistication with practical considerations such as staff training, sterilization processes, and interoperability. Early adopters are focusing on modalities that enhance visualization-higher-resolution sensors, three-dimensional imaging, and four K systems-while payers and providers seek evidence of clinical and operational value. Consequently, stakeholders must navigate a complex convergence of clinical imperatives, regulatory expectations, and capital planning cycles as they evaluate next-generation endoscopy visualization platforms.
How converging advances in imaging resolution, AI assistance, and infection-control imperatives are reshaping procurement, clinical adoption, and competitive differentiation
The endoscopy visualization landscape is undergoing transformative shifts driven by advances in imaging technology, renewed emphasis on infection prevention, and the emergence of software-enabled diagnostic support. Higher-resolution outputs such as four K and three D systems are redefining what clinicians expect from visual feedback during complex procedures, while AI algorithms are beginning to offer real-time lesion characterization and decision support. At the same time, heightened scrutiny of reusable instrument reprocessing has accelerated interest in single-use alternatives and hybrid system designs that promise reduced turnover time and lower cross-contamination risk.
In parallel, care delivery is decentralizing; ambulatory surgical centers and specialty clinics are increasingly performing procedures that were once hospital-centric, requiring vendors to adapt form factors and service models to diverse end user environments. These converging dynamics favor flexible commercial strategies that pair hardware innovation with robust service offerings, regulatory preparedness, and training programs designed to shorten time to clinical utility. Consequently, competitive advantage will accrue to firms that can demonstrate measurable improvements in diagnostic confidence, throughput, and total cost of ownership across varied clinical settings.
Assessing how the 2025 United States tariff adjustments have reshaped component sourcing, manufacturing footprints, and procurement calculus within endoscopy visualization supply chains
Tariff policy shifts imposed by the United States in 2025 have introduced a new layer of complexity to global supply chains for medical imaging and endoscopy components. Increased duties on certain optical components, electronics, and imported assemblies have pressured manufacturers to reassess sourcing strategies and cost allocation. In response, some suppliers accelerated nearshoring or regional manufacturing partnerships to mitigate exposure to tariffs, while others absorbed incremental costs in the short term to preserve market access and contractual commitments.
These adjustments have immediate and medium-term implications for pricing strategies, product configuration choices, and inventory management. Providers weighing capital acquisitions must now factor potential customs duties and lead‑time variability into procurement timelines. Moreover, regulatory and quality assurance requirements for component substitution or supplier changes can lengthen product qualification cycles. Hence, successful vendors and health systems will be those that transparently communicate supply chain resilience, offer modular product options that accommodate regional sourcing, and work collaboratively to minimize operational disruption while maintaining clinical performance standards.
In-depth segmentation-driven perspectives showing how product type, clinical application, care setting, and imaging modality interact to shape procurement priorities and adoption patterns
A detailed segmentation lens reveals nuanced opportunities and constraints across product type, application, end user, and modality that should guide strategic planning. Product type dynamics vary between capsule endoscope systems, flexible endoscope systems, hybrid endoscope systems, rigid endoscope systems, and single-use endoscope systems; within that, flexible solutions split into reusable flexible endoscope systems and single-use flexible endoscope systems, and rigid alternatives similarly differentiate into reusable rigid endoscope systems and single-use rigid endoscope systems. Application areas span ear nose throat, gastroenterology, gynecology, orthopedics, and urology, each with distinct visualization requirements and procedural volumes. End users include ambulatory surgical centers, clinics, and hospitals, where clinics further divide into general clinics and specialty clinics and hospitals further divide into private hospitals and public hospitals, shaping purchasing behavior and service expectations. Modality preferences cover four K systems, three D systems, and two D systems, reflecting clinician demand for higher resolution and depth perception in particular procedural contexts.
Taken together, these segmentation dimensions illustrate that no single strategy fits all environments. For example, gastroenterology centers with high throughput prioritize durability and sterilization efficiency, favoring reusable flexible systems when reprocessing infrastructure is mature, whereas lower-volume specialty clinics may opt for single-use flexible devices to avoid reprocessing overhead. Similarly, the choice between two D, three D, and four K modalities often represents a trade-off between upfront capital intensity and incremental clinical benefit, so vendors need modular upgrade paths and financing models to address heterogeneous buyer profiles across ambulatory surgical centers, clinics, and public and private hospitals.
How regional regulatory regimes, purchasing architectures, and clinical infrastructure variations drive distinct adoption pathways across the Americas, Europe, Middle East & Africa, and Asia-Pacific
Regional dynamics shape technology adoption and commercial strategies in ways that reflect local reimbursement policies, regulatory environments, and care delivery models. In the Americas, centralized purchasing practices in large hospital systems and a growing network of ambulatory surgical centers create opportunities for bundled procurement and service contracts, while innovation adoption often accelerates where reimbursement supports advanced diagnostic procedures. In Europe, Middle East & Africa, diverse regulatory regimes and variable capital budgets necessitate flexible entry strategies and evidence packages that address country-level concerns about cost-effectiveness and training.
Asia-Pacific markets present a heterogeneous picture with pockets of rapid adoption driven by rising procedural volumes, investment in tertiary care infrastructure, and strong domestic manufacturing ecosystems. Across these regions, vendors must balance standardization with localization: standard hardware platforms can reduce manufacturing complexity, yet software customization, language support, and regional service offerings drive clinician satisfaction and long-term retention. Therefore, commercial models that combine regional supply resilience, focused clinical evidence, and scalable training programs are most likely to succeed across the Americas, Europe, Middle East & Africa, and Asia-Pacific.
Competitive landscape analysis emphasizing how legacy manufacturers, specialist entrants, and software innovators are shaping value propositions and aftermarket economics
Competitive dynamics in the endoscopy visualization space are defined by a mix of legacy medical device manufacturers, emerging specialist firms, and technology companies expanding into medical imaging with software and sensor innovations. Established firms typically leverage deep service networks and validated clinical data to maintain installed base relationships, while specialist entrants compete by targeting niche applications or offering differentiated value in areas such as single-use devices, modular optics, or AI-enabled image analysis.
Strategic partnerships and M&A remain important mechanisms for capability acquisition, allowing companies to combine hardware scale with software expertise or to secure regional distribution channels. Additionally, companies that prioritize lifecycle support, predictable consumable pricing, and clinician training programs tend to outperform peers on customer retention. Investors and corporate strategists should therefore evaluate not just product roadmaps but also after-sales service models, regulatory track records, and the ability to integrate third-party analytics platforms, because these factors ultimately determine how quickly new visualization technologies translate into measurable clinical adoption.
Actionable directives for vendors and providers to operationalize imaging innovation through interoperability, evidence generation, resilience, and outcome-focused commercial models
Industry leaders can act now to convert technological potential into sustained clinical and commercial value by prioritizing interoperability, flexible procurement options, and demonstrable clinical outcomes. Vendors should build modular platforms that accommodate upgrades from two D to three D or four K modalities and design service contracts that align incentives around uptime, training, and consumable cost predictability. In tandem, providers should reassess sterilization capacity and workflow design to determine where single-use instruments offer net operational advantages versus investments in reusable device reprocessing.
Moreover, stakeholders should invest in robust clinical evidence generation that spans real-world performance in ambulatory surgical centers, clinics, and both private and public hospital settings. Collaborative pilots that embed imaging systems with AI decision support and measure diagnostic yield, procedure duration, and downstream patient outcomes will accelerate payer acceptance and inform reimbursement discussions. Finally, supply chain resilience must be addressed proactively through diversified sourcing and regional manufacturing partnerships to mitigate the effects of trade policy volatility and component constraints.
A concise description of the rigorous multi-method research approach combining primary stakeholder interviews, technical reviews, and supply chain analysis to validate insights
This analysis draws from a multi-method research approach combining primary interviews, secondary literature reviews, technology assessments, and supply chain traceability mapping to ensure both depth and accuracy. Primary research included structured conversations with clinical leaders across ambulatory surgical centers, specialty and general clinics, and private and public hospitals, together with engagements with procurement officers and supply chain executives to validate procurement drivers and operational constraints. Secondary sources encompassed regulatory filings, peer-reviewed clinical studies, device clearance documentation, and manufacturer technical specifications to triangulate product capabilities and clinical use patterns.
To assess supply chain and tariff impacts, the methodology integrated customs data, supplier disclosure analysis, and scenario planning exercises with operations leaders to model sourcing adjustments and lead-time sensitivities. Throughout, emphasis was placed on qualitative validation and cross-referencing of claims to minimize bias and ensure that recommendations are grounded in reproducible evidence. Where applicable, data were anonymized and aggregated to preserve confidentiality while enabling comparative insights across product types, applications, end users, and modalities.
Closing synthesis highlighting the imperative for evidence-based adoption, scalable service models, and supply chain robustness to realize imaging-driven clinical improvements
The convergence of higher-resolution imaging, software-enabled decision support, and evolving infection-control expectations means endoscopy visualization is poised for meaningful evolution in clinical practice. Providers and vendors who align technological capability with pragmatic considerations-training, sterilization, total cost of ownership, and supply chain resilience-will be best positioned to capture clinical value and drive sustained adoption. Importantly, segmentation by product type, application, care setting, and modality reveals that tailored strategies, not one-size-fits-all solutions, are essential for realizing the potential of advanced visualization.
In sum, the path forward requires coordinated investments in clinical evidence, interoperable architectures, and flexible commercial models that accommodate regional regulatory and reimbursement heterogeneity. By focusing on demonstrable outcomes, scalability across ambulatory and hospital settings, and transparent supply chain practices, stakeholders can translate innovation into measurable improvements in diagnostic confidence, procedure efficiency, and patient safety.
Note: PDF & Excel + Online Access - 1 Year
Framing the era of imaging-led procedural care where clinical outcomes, workflow integration, and infection control jointly determine endoscopy system selection
Endoscopy visualization is at the intersection of optics, digital imaging, and clinical workflow optimization, driving demand for solutions that improve diagnostic accuracy and procedural efficiency. Clinicians and procurement leaders are evaluating systems not only for image fidelity and ergonomics but also for integration with electronic health records, AI-assisted analytics, and infection control protocols. As a result, adoption decisions increasingly hinge on a system’s ability to deliver reproducible outcomes across inpatient and outpatient environments while minimizing lifecycle costs and downtime.
Looking ahead, the landscape will be determined by how vendors balance technological sophistication with practical considerations such as staff training, sterilization processes, and interoperability. Early adopters are focusing on modalities that enhance visualization-higher-resolution sensors, three-dimensional imaging, and four K systems-while payers and providers seek evidence of clinical and operational value. Consequently, stakeholders must navigate a complex convergence of clinical imperatives, regulatory expectations, and capital planning cycles as they evaluate next-generation endoscopy visualization platforms.
How converging advances in imaging resolution, AI assistance, and infection-control imperatives are reshaping procurement, clinical adoption, and competitive differentiation
The endoscopy visualization landscape is undergoing transformative shifts driven by advances in imaging technology, renewed emphasis on infection prevention, and the emergence of software-enabled diagnostic support. Higher-resolution outputs such as four K and three D systems are redefining what clinicians expect from visual feedback during complex procedures, while AI algorithms are beginning to offer real-time lesion characterization and decision support. At the same time, heightened scrutiny of reusable instrument reprocessing has accelerated interest in single-use alternatives and hybrid system designs that promise reduced turnover time and lower cross-contamination risk.
In parallel, care delivery is decentralizing; ambulatory surgical centers and specialty clinics are increasingly performing procedures that were once hospital-centric, requiring vendors to adapt form factors and service models to diverse end user environments. These converging dynamics favor flexible commercial strategies that pair hardware innovation with robust service offerings, regulatory preparedness, and training programs designed to shorten time to clinical utility. Consequently, competitive advantage will accrue to firms that can demonstrate measurable improvements in diagnostic confidence, throughput, and total cost of ownership across varied clinical settings.
Assessing how the 2025 United States tariff adjustments have reshaped component sourcing, manufacturing footprints, and procurement calculus within endoscopy visualization supply chains
Tariff policy shifts imposed by the United States in 2025 have introduced a new layer of complexity to global supply chains for medical imaging and endoscopy components. Increased duties on certain optical components, electronics, and imported assemblies have pressured manufacturers to reassess sourcing strategies and cost allocation. In response, some suppliers accelerated nearshoring or regional manufacturing partnerships to mitigate exposure to tariffs, while others absorbed incremental costs in the short term to preserve market access and contractual commitments.
These adjustments have immediate and medium-term implications for pricing strategies, product configuration choices, and inventory management. Providers weighing capital acquisitions must now factor potential customs duties and lead‑time variability into procurement timelines. Moreover, regulatory and quality assurance requirements for component substitution or supplier changes can lengthen product qualification cycles. Hence, successful vendors and health systems will be those that transparently communicate supply chain resilience, offer modular product options that accommodate regional sourcing, and work collaboratively to minimize operational disruption while maintaining clinical performance standards.
In-depth segmentation-driven perspectives showing how product type, clinical application, care setting, and imaging modality interact to shape procurement priorities and adoption patterns
A detailed segmentation lens reveals nuanced opportunities and constraints across product type, application, end user, and modality that should guide strategic planning. Product type dynamics vary between capsule endoscope systems, flexible endoscope systems, hybrid endoscope systems, rigid endoscope systems, and single-use endoscope systems; within that, flexible solutions split into reusable flexible endoscope systems and single-use flexible endoscope systems, and rigid alternatives similarly differentiate into reusable rigid endoscope systems and single-use rigid endoscope systems. Application areas span ear nose throat, gastroenterology, gynecology, orthopedics, and urology, each with distinct visualization requirements and procedural volumes. End users include ambulatory surgical centers, clinics, and hospitals, where clinics further divide into general clinics and specialty clinics and hospitals further divide into private hospitals and public hospitals, shaping purchasing behavior and service expectations. Modality preferences cover four K systems, three D systems, and two D systems, reflecting clinician demand for higher resolution and depth perception in particular procedural contexts.
Taken together, these segmentation dimensions illustrate that no single strategy fits all environments. For example, gastroenterology centers with high throughput prioritize durability and sterilization efficiency, favoring reusable flexible systems when reprocessing infrastructure is mature, whereas lower-volume specialty clinics may opt for single-use flexible devices to avoid reprocessing overhead. Similarly, the choice between two D, three D, and four K modalities often represents a trade-off between upfront capital intensity and incremental clinical benefit, so vendors need modular upgrade paths and financing models to address heterogeneous buyer profiles across ambulatory surgical centers, clinics, and public and private hospitals.
How regional regulatory regimes, purchasing architectures, and clinical infrastructure variations drive distinct adoption pathways across the Americas, Europe, Middle East & Africa, and Asia-Pacific
Regional dynamics shape technology adoption and commercial strategies in ways that reflect local reimbursement policies, regulatory environments, and care delivery models. In the Americas, centralized purchasing practices in large hospital systems and a growing network of ambulatory surgical centers create opportunities for bundled procurement and service contracts, while innovation adoption often accelerates where reimbursement supports advanced diagnostic procedures. In Europe, Middle East & Africa, diverse regulatory regimes and variable capital budgets necessitate flexible entry strategies and evidence packages that address country-level concerns about cost-effectiveness and training.
Asia-Pacific markets present a heterogeneous picture with pockets of rapid adoption driven by rising procedural volumes, investment in tertiary care infrastructure, and strong domestic manufacturing ecosystems. Across these regions, vendors must balance standardization with localization: standard hardware platforms can reduce manufacturing complexity, yet software customization, language support, and regional service offerings drive clinician satisfaction and long-term retention. Therefore, commercial models that combine regional supply resilience, focused clinical evidence, and scalable training programs are most likely to succeed across the Americas, Europe, Middle East & Africa, and Asia-Pacific.
Competitive landscape analysis emphasizing how legacy manufacturers, specialist entrants, and software innovators are shaping value propositions and aftermarket economics
Competitive dynamics in the endoscopy visualization space are defined by a mix of legacy medical device manufacturers, emerging specialist firms, and technology companies expanding into medical imaging with software and sensor innovations. Established firms typically leverage deep service networks and validated clinical data to maintain installed base relationships, while specialist entrants compete by targeting niche applications or offering differentiated value in areas such as single-use devices, modular optics, or AI-enabled image analysis.
Strategic partnerships and M&A remain important mechanisms for capability acquisition, allowing companies to combine hardware scale with software expertise or to secure regional distribution channels. Additionally, companies that prioritize lifecycle support, predictable consumable pricing, and clinician training programs tend to outperform peers on customer retention. Investors and corporate strategists should therefore evaluate not just product roadmaps but also after-sales service models, regulatory track records, and the ability to integrate third-party analytics platforms, because these factors ultimately determine how quickly new visualization technologies translate into measurable clinical adoption.
Actionable directives for vendors and providers to operationalize imaging innovation through interoperability, evidence generation, resilience, and outcome-focused commercial models
Industry leaders can act now to convert technological potential into sustained clinical and commercial value by prioritizing interoperability, flexible procurement options, and demonstrable clinical outcomes. Vendors should build modular platforms that accommodate upgrades from two D to three D or four K modalities and design service contracts that align incentives around uptime, training, and consumable cost predictability. In tandem, providers should reassess sterilization capacity and workflow design to determine where single-use instruments offer net operational advantages versus investments in reusable device reprocessing.
Moreover, stakeholders should invest in robust clinical evidence generation that spans real-world performance in ambulatory surgical centers, clinics, and both private and public hospital settings. Collaborative pilots that embed imaging systems with AI decision support and measure diagnostic yield, procedure duration, and downstream patient outcomes will accelerate payer acceptance and inform reimbursement discussions. Finally, supply chain resilience must be addressed proactively through diversified sourcing and regional manufacturing partnerships to mitigate the effects of trade policy volatility and component constraints.
A concise description of the rigorous multi-method research approach combining primary stakeholder interviews, technical reviews, and supply chain analysis to validate insights
This analysis draws from a multi-method research approach combining primary interviews, secondary literature reviews, technology assessments, and supply chain traceability mapping to ensure both depth and accuracy. Primary research included structured conversations with clinical leaders across ambulatory surgical centers, specialty and general clinics, and private and public hospitals, together with engagements with procurement officers and supply chain executives to validate procurement drivers and operational constraints. Secondary sources encompassed regulatory filings, peer-reviewed clinical studies, device clearance documentation, and manufacturer technical specifications to triangulate product capabilities and clinical use patterns.
To assess supply chain and tariff impacts, the methodology integrated customs data, supplier disclosure analysis, and scenario planning exercises with operations leaders to model sourcing adjustments and lead-time sensitivities. Throughout, emphasis was placed on qualitative validation and cross-referencing of claims to minimize bias and ensure that recommendations are grounded in reproducible evidence. Where applicable, data were anonymized and aggregated to preserve confidentiality while enabling comparative insights across product types, applications, end users, and modalities.
Closing synthesis highlighting the imperative for evidence-based adoption, scalable service models, and supply chain robustness to realize imaging-driven clinical improvements
The convergence of higher-resolution imaging, software-enabled decision support, and evolving infection-control expectations means endoscopy visualization is poised for meaningful evolution in clinical practice. Providers and vendors who align technological capability with pragmatic considerations-training, sterilization, total cost of ownership, and supply chain resilience-will be best positioned to capture clinical value and drive sustained adoption. Importantly, segmentation by product type, application, care setting, and modality reveals that tailored strategies, not one-size-fits-all solutions, are essential for realizing the potential of advanced visualization.
In sum, the path forward requires coordinated investments in clinical evidence, interoperable architectures, and flexible commercial models that accommodate regional regulatory and reimbursement heterogeneity. By focusing on demonstrable outcomes, scalability across ambulatory and hospital settings, and transparent supply chain practices, stakeholders can translate innovation into measurable improvements in diagnostic confidence, procedure efficiency, and patient safety.
Note: PDF & Excel + Online Access - 1 Year
Table of Contents
189 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. Integration of artificial intelligence for real-time tissue characterization and lesion detection during endoscopic procedures
- 5.2. Adoption of high-definition 4K and 3D imaging systems to improve precision in minimally invasive surgeries
- 5.3. Utilization of augmented reality overlays for enhanced navigation and orientation in complex endoscopy procedures
- 5.4. Development of disposable single-use visualization endoscopes to reduce cross-contamination and infection risk
- 5.5. Expansion of wireless capsule endoscopy with advanced microcamera sensors for noninvasive gastrointestinal diagnosis
- 5.6. Implementation of cloud-based endoscopy data management platforms for streamlined case review and collaborative diagnosis
- 5.7. Incorporation of multispectral imaging techniques to distinguish between healthy and abnormal mucosal tissues in real time
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Endoscopy Visualization Systems Market, by Product Type
- 8.1. Capsule Endoscope Systems
- 8.2. Flexible Endoscope Systems
- 8.2.1. Reusable Flexible Endoscope Systems
- 8.2.2. Single-Use Flexible Endoscope Systems
- 8.3. Hybrid Endoscope Systems
- 8.4. Rigid Endoscope Systems
- 8.4.1. Reusable Rigid Endoscope Systems
- 8.4.2. Single-Use Rigid Endoscope Systems
- 8.5. Single-Use Endoscope Systems
- 9. Endoscopy Visualization Systems Market, by Application
- 9.1. Ear Nose Throat
- 9.2. Gastroenterology
- 9.3. Gynecology
- 9.4. Orthopedics
- 9.5. Urology
- 10. Endoscopy Visualization Systems Market, by End User
- 10.1. Ambulatory Surgical Centers
- 10.2. Clinics
- 10.2.1. General Clinics
- 10.2.2. Specialty Clinics
- 10.3. Hospitals
- 10.3.1. Private Hospitals
- 10.3.2. Public Hospitals
- 11. Endoscopy Visualization Systems Market, by Modality
- 11.1. Four K Systems
- 11.2. Three D Systems
- 11.3. Two D Systems
- 12. Endoscopy Visualization Systems 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. Endoscopy Visualization Systems Market, by Group
- 13.1. ASEAN
- 13.2. GCC
- 13.3. European Union
- 13.4. BRICS
- 13.5. G7
- 13.6. NATO
- 14. Endoscopy Visualization Systems 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. Olympus Corporation
- 15.3.2. KARL STORZ SE & Co. KG
- 15.3.3. Stryker Corporation
- 15.3.4. Fujifilm Holdings Corporation
- 15.3.5. HOYA CORPORATION
- 15.3.6. Richard Wolf GmbH
- 15.3.7. Medtronic plc
- 15.3.8. Boston Scientific Corporation
- 15.3.9. Johnson & Johnson
- 15.3.10. CONMED Corporation
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