Robotic Endoscopy Devices Market by Device Type (Diagnostic, Therapeutic), Technology (Capsule Endoscope, Flexible Robotic Endoscope, Rigid Robotic Endoscope), Application, End User - Global Forecast 2025-2032
Description
The Robotic Endoscopy Devices Market was valued at USD 3.09 billion in 2024 and is projected to grow to USD 3.70 billion in 2025, with a CAGR of 19.18%, reaching USD 12.59 billion by 2032.
An accessible overview of how recent technological and clinical advances are redefining procedural standards and stakeholder priorities within robotic endoscopy
Robotic endoscopy is reshaping diagnostic and therapeutic workflows by combining precision mechanics, advanced imaging, and data-rich software to extend clinician capability and improve patient experience. Recent advances in actuator miniaturization, sensor fusion, and disposable device concepts have shifted the technology conversation from incremental enhancements to the prospect of fundamentally different care pathways. As a result, stakeholders across clinical practice, device manufacturing, and healthcare procurement are reassessing procedural protocols, capital allocation, and partnership models.
This introduction outlines the landscape drivers that matter to leaders evaluating investment or adoption of robotic endoscopy systems. It synthesizes the clinical imperatives that motivate innovation, including the need for less invasive access, improved diagnostic yield, and reduced procedural variability. The narrative also highlights the convergence of complementary technologies such as capsule endoscopy, flexible robotics, and advanced visualization which together are forming new categories of solutions. The intent here is to set a practical frame for reading the deeper analyses that follow, focusing on strategic implications rather than technical minutiae.
A clear exposition of the major systemic shifts transforming product design, clinical adoption, and partnership models across the robotic endoscopy ecosystem
The landscape for robotic endoscopy devices is undergoing a series of transformative shifts driven by technology maturation, clinical evidence development, and evolving care delivery models. Miniaturization and materials innovation have enabled new form factors, making capsule-based and highly flexible robotic platforms clinically feasible. Concurrently, the integration of artificial intelligence into image analysis and navigation is reducing cognitive load for clinicians and enabling earlier, more reliable detection of pathology.
Procurement models are also changing as ambulatory and outpatient settings expand their procedural repertoire, prompting manufacturers to rethink sterilization, service, and warranty propositions. Regulatory pathways are adapting to accommodate software-driven modalities and modular device architectures, encouraging iterative product improvements rather than monolithic product launches. Additionally, partnerships across medical imaging, telehealth, and robotics ecosystems are accelerating co-development programs, creating blended solutions that couple procedure automation with remote expert oversight. These shifts collectively move the market from a device-centric to a systems-centric mindset, where interoperability, clinical workflows, and value-based outcomes determine adoption more than hardware specifications alone.
A focused analysis of how the 2025 tariff measures reshaped sourcing, manufacturing strategy, and procurement dynamics for robotic endoscopy device stakeholders
The tariff actions implemented by the United States in 2025 have introduced an operational inflection point for global supply chains serving robotic endoscopy device manufacturers. Tariff-driven cost pressures have prompted procurement teams to reassess component sourcing and supplier footprints, with device makers pursuing a mix of mitigation strategies that include tariff reclassification petitions, supplier dual-sourcing, and selective nearshoring. These responses are creating a new calculus for manufacturers weighing the trade-offs between cost, lead time, and regulatory compliance associated with alternate suppliers.
In parallel, clinical customers and hospital systems are evaluating total cost of ownership more closely, accounting for potential import duties and logistical complexity when comparing competing platforms. The tariffs have accelerated conversations about domestic manufacturing and contract manufacturing partnerships in countries with favorable trade arrangements, and they have increased the importance of tariff engineering as a design consideration. Regulatory and customs compliance functions within companies have also been stretched, requiring more rigorous documentation of country of origin, bill of materials traceability, and tariff code assessments. Over time, these pressures are influencing product roadmaps, with a growing emphasis on component standardization and modular architectures that facilitate local assembly and reduce exposure to trade measures.
A detailed synthesis of how device type, clinical application, core technologies, user settings, and sales channels shape strategic priorities and development choices
Segmentation clarity reveals how clinical use cases, device capabilities, and end-user requirements intersect to shape product strategies. Based on device type, analyses consider Diagnostic, which is further differentiated into Biopsy and Imaging capabilities, and Therapeutic, which is further parsed across Ablation, Hemostasis, and Resection modalities, illuminating how design trade-offs vary between tissue sampling and interventional treatment. Based on application, the directional emphasis across Bronchial, Gastrointestinal including Lower Gastrointestinal and Upper Gastrointestinal subdomains, Otolaryngological, and Urological applications shows where device ergonomics and visualization demands diverge and where clinical training pathways must be tailored.
Based on technology, the taxonomy distinguishes Capsule Endoscope, Flexible Robotic Endoscope, and Rigid Robotic Endoscope platforms, each presenting unique constraints around power delivery, data bandwidth, and disposability. Based on end user, the competitive and operational requirements differ significantly between Ambulatory Surgical Centers, Clinics, Hospitals, and Research Institutes, affecting service models, purchasing cycles, and clinical support needs. Based on sales channel, differentiation between Direct Sales and Distribution governs margin structures, customer intimacy, and post-sale service commitments. Understanding these intersecting segment definitions is essential to prioritize R&D bets, align go-to-market motions, and design clinical evidence generation plans that resonate with specific purchasing constituencies.
A comparative view of how regional healthcare systems, procurement practices, and industrial policies influence clinical adoption and commercial strategies for robotic endoscopy
Regional dynamics are materially influencing adoption patterns and strategic priorities for robotic endoscopy companies. In the Americas, investment in outpatient infrastructure and a pronounced focus on value-based care have elevated interest in systems that reduce procedure time and enable safer, same-day interventions. Reimbursement pathways and hospital procurement processes in this region create both incentives and constraints that vendors must navigate through robust clinical data and targeted payer engagement.
In Europe, Middle East & Africa, the interplay between centralized health systems, regulatory harmonization efforts, and diverse procurement practices results in a mosaic of adoption timelines; manufacturers need adaptable regulatory strategies and flexible commercial models to serve public and private providers. In Asia-Pacific, rapid clinical uptake is being driven by substantial private sector facility growth, a strong appetite for tech-enabled solutions, and active domestic industrial policies that sometimes favor local manufacturers. Across regions, cross-border regulatory convergence, clinical training programs, and strategic partnerships are pivotal levers for scaling adoption and capturing the full clinical potential of robotic endoscopy innovations.
An incisive look at how industry leaders are building competitive moats through clinical evidence, platform architectures, and commercial model innovation
Leading companies in the robotic endoscopy space are converging on several consistent strategic plays: vertical integration of imaging, navigation, and robotic actuation; purposeful accumulation of clinical evidence through multicenter studies and registry programs; and selective partnerships to extend distribution or clinical reach. Companies are also experimenting with as-a-service models for high-capital systems, bundling devices with maintenance, analytics, and consumables to stabilize revenue and deepen customer relationships. Intellectual property portfolios and modular platform design are being leveraged to protect competitive advantage while enabling incremental software-enabled improvements that can be deployed under existing regulatory clearances.
Competitive positioning increasingly hinges on ecosystem orchestration rather than single-product superiority. Firms that can align clinical workflow support, training services, and outcome-tracking tools alongside their devices create stronger switching costs for customers. At the same time, smaller innovators are attracting attention through targeted niche solutions-such as capsule platforms for specific gastrointestinal indications or highly flexible tools tailored for bronchial navigation-creating a bifurcated competitive environment where scale and specialization coexist. Investors and corporate development teams are therefore prioritizing opportunities that offer either clear path to scale or defensible specialization backed by clinical differentiation.
Actionable, prioritized recommendations for leaders to strengthen supply chains, accelerate clinical validation, and optimize commercial models for scalable adoption
Industry leaders should prioritize a dual-track strategy that balances near-term operational resilience with longer-term platform differentiation. In the near term, companies should secure supply chain flexibility by diversifying qualified suppliers, enhancing bill-of-materials traceability, and pursuing tariff mitigation strategies where appropriate. Concurrently, focus on modularity in hardware and software will enable faster iteration cycles and reduce the cost of compliance for incremental improvements. Investing in robust clinical evidence programs that demonstrate procedure-level benefits and patient-centered outcomes will accelerate reimbursement dialogues and reduce purchaser risk aversion.
Commercially, firms should tailor go-to-market approaches to the specific needs of hospitals, ambulatory centers, and clinics, aligning direct sales efforts with high-touch clinical training and channel partnerships for broad geographic coverage. Strategic partnerships with imaging and software vendors can create bundled value propositions that are harder to replicate. Finally, leadership teams should consider alternative commercial constructs such as managed equipment services, outcome-based pricing pilots, and subscription models for analytics to unlock new adoption vectors and smoother revenue streams. Executed together, these moves will strengthen resilience and position companies to benefit from the structural changes reshaping endoscopy care delivery.
A transparent description of the mixed-methods research approach used to compile evidence, validate themes, and ensure practical relevance for decision-makers
The research underpinning this executive analysis combined primary and secondary methods to ensure rigorous, multi-dimensional validation of insights. Primary research included structured interviews with clinical leaders, procurement specialists, and senior executives involved in product strategy, along with observational reviews of procedural workflows where available. Secondary research encompassed peer-reviewed clinical literature, regulatory filings, patent records, and manufacturer technical documentation to triangulate technology trends and device capabilities.
Synthesis processes involved cross-validation of qualitative insights with document-based evidence, thematic coding of interview transcripts to identify recurring operational challenges and innovation priorities, and mapping of regulatory milestones against product introductions. The methodology acknowledges inherent limitations, including variability in clinical practice across regions and uneven public disclosure of proprietary cost structures. To mitigate these constraints, findings were stress-tested with multiple stakeholders and framed conservatively to reflect practice realities rather than vendor claims. The resulting approach balances depth of technical understanding with pragmatic relevance for decision-makers.
A succinct conclusion that synthesizes strategic priorities and clarifies the organizational capabilities needed to capture value from advancements in robotic endoscopy
The robotic endoscopy device landscape is at a strategic inflection point where technological capability, clinical evidence, and commercial model innovation converge to create new opportunities and operational challenges. Advances in capsule, flexible, and rigid robotic platforms are enabling clinicians to reconsider procedural boundaries, while regulatory and procurement dynamics are shaping how and where these technologies scale. Supply chain pressures, including trade measures and component sourcing complexity, are forcing companies to adapt their manufacturing logic and design priorities to preserve competitiveness.
For stakeholders considering engagement-whether through procurement, partnership, investment, or clinical adoption-the imperative is to evaluate opportunities through a multi-dimensional lens that integrates clinical outcomes, economic implications, and operational feasibility. Organizations that align product roadmaps with pragmatic regulatory strategies, resilient supply chains, and targeted evidence generation will be best positioned to translate innovation into sustainable clinical impact and commercial success. The most successful entrants will be those that treat robotic endoscopy not as an isolated product play but as a systems-level offering that must harmonize technology, clinical workflows, and service delivery.
Please Note: PDF & Excel + Online Access - 1 Year
An accessible overview of how recent technological and clinical advances are redefining procedural standards and stakeholder priorities within robotic endoscopy
Robotic endoscopy is reshaping diagnostic and therapeutic workflows by combining precision mechanics, advanced imaging, and data-rich software to extend clinician capability and improve patient experience. Recent advances in actuator miniaturization, sensor fusion, and disposable device concepts have shifted the technology conversation from incremental enhancements to the prospect of fundamentally different care pathways. As a result, stakeholders across clinical practice, device manufacturing, and healthcare procurement are reassessing procedural protocols, capital allocation, and partnership models.
This introduction outlines the landscape drivers that matter to leaders evaluating investment or adoption of robotic endoscopy systems. It synthesizes the clinical imperatives that motivate innovation, including the need for less invasive access, improved diagnostic yield, and reduced procedural variability. The narrative also highlights the convergence of complementary technologies such as capsule endoscopy, flexible robotics, and advanced visualization which together are forming new categories of solutions. The intent here is to set a practical frame for reading the deeper analyses that follow, focusing on strategic implications rather than technical minutiae.
A clear exposition of the major systemic shifts transforming product design, clinical adoption, and partnership models across the robotic endoscopy ecosystem
The landscape for robotic endoscopy devices is undergoing a series of transformative shifts driven by technology maturation, clinical evidence development, and evolving care delivery models. Miniaturization and materials innovation have enabled new form factors, making capsule-based and highly flexible robotic platforms clinically feasible. Concurrently, the integration of artificial intelligence into image analysis and navigation is reducing cognitive load for clinicians and enabling earlier, more reliable detection of pathology.
Procurement models are also changing as ambulatory and outpatient settings expand their procedural repertoire, prompting manufacturers to rethink sterilization, service, and warranty propositions. Regulatory pathways are adapting to accommodate software-driven modalities and modular device architectures, encouraging iterative product improvements rather than monolithic product launches. Additionally, partnerships across medical imaging, telehealth, and robotics ecosystems are accelerating co-development programs, creating blended solutions that couple procedure automation with remote expert oversight. These shifts collectively move the market from a device-centric to a systems-centric mindset, where interoperability, clinical workflows, and value-based outcomes determine adoption more than hardware specifications alone.
A focused analysis of how the 2025 tariff measures reshaped sourcing, manufacturing strategy, and procurement dynamics for robotic endoscopy device stakeholders
The tariff actions implemented by the United States in 2025 have introduced an operational inflection point for global supply chains serving robotic endoscopy device manufacturers. Tariff-driven cost pressures have prompted procurement teams to reassess component sourcing and supplier footprints, with device makers pursuing a mix of mitigation strategies that include tariff reclassification petitions, supplier dual-sourcing, and selective nearshoring. These responses are creating a new calculus for manufacturers weighing the trade-offs between cost, lead time, and regulatory compliance associated with alternate suppliers.
In parallel, clinical customers and hospital systems are evaluating total cost of ownership more closely, accounting for potential import duties and logistical complexity when comparing competing platforms. The tariffs have accelerated conversations about domestic manufacturing and contract manufacturing partnerships in countries with favorable trade arrangements, and they have increased the importance of tariff engineering as a design consideration. Regulatory and customs compliance functions within companies have also been stretched, requiring more rigorous documentation of country of origin, bill of materials traceability, and tariff code assessments. Over time, these pressures are influencing product roadmaps, with a growing emphasis on component standardization and modular architectures that facilitate local assembly and reduce exposure to trade measures.
A detailed synthesis of how device type, clinical application, core technologies, user settings, and sales channels shape strategic priorities and development choices
Segmentation clarity reveals how clinical use cases, device capabilities, and end-user requirements intersect to shape product strategies. Based on device type, analyses consider Diagnostic, which is further differentiated into Biopsy and Imaging capabilities, and Therapeutic, which is further parsed across Ablation, Hemostasis, and Resection modalities, illuminating how design trade-offs vary between tissue sampling and interventional treatment. Based on application, the directional emphasis across Bronchial, Gastrointestinal including Lower Gastrointestinal and Upper Gastrointestinal subdomains, Otolaryngological, and Urological applications shows where device ergonomics and visualization demands diverge and where clinical training pathways must be tailored.
Based on technology, the taxonomy distinguishes Capsule Endoscope, Flexible Robotic Endoscope, and Rigid Robotic Endoscope platforms, each presenting unique constraints around power delivery, data bandwidth, and disposability. Based on end user, the competitive and operational requirements differ significantly between Ambulatory Surgical Centers, Clinics, Hospitals, and Research Institutes, affecting service models, purchasing cycles, and clinical support needs. Based on sales channel, differentiation between Direct Sales and Distribution governs margin structures, customer intimacy, and post-sale service commitments. Understanding these intersecting segment definitions is essential to prioritize R&D bets, align go-to-market motions, and design clinical evidence generation plans that resonate with specific purchasing constituencies.
A comparative view of how regional healthcare systems, procurement practices, and industrial policies influence clinical adoption and commercial strategies for robotic endoscopy
Regional dynamics are materially influencing adoption patterns and strategic priorities for robotic endoscopy companies. In the Americas, investment in outpatient infrastructure and a pronounced focus on value-based care have elevated interest in systems that reduce procedure time and enable safer, same-day interventions. Reimbursement pathways and hospital procurement processes in this region create both incentives and constraints that vendors must navigate through robust clinical data and targeted payer engagement.
In Europe, Middle East & Africa, the interplay between centralized health systems, regulatory harmonization efforts, and diverse procurement practices results in a mosaic of adoption timelines; manufacturers need adaptable regulatory strategies and flexible commercial models to serve public and private providers. In Asia-Pacific, rapid clinical uptake is being driven by substantial private sector facility growth, a strong appetite for tech-enabled solutions, and active domestic industrial policies that sometimes favor local manufacturers. Across regions, cross-border regulatory convergence, clinical training programs, and strategic partnerships are pivotal levers for scaling adoption and capturing the full clinical potential of robotic endoscopy innovations.
An incisive look at how industry leaders are building competitive moats through clinical evidence, platform architectures, and commercial model innovation
Leading companies in the robotic endoscopy space are converging on several consistent strategic plays: vertical integration of imaging, navigation, and robotic actuation; purposeful accumulation of clinical evidence through multicenter studies and registry programs; and selective partnerships to extend distribution or clinical reach. Companies are also experimenting with as-a-service models for high-capital systems, bundling devices with maintenance, analytics, and consumables to stabilize revenue and deepen customer relationships. Intellectual property portfolios and modular platform design are being leveraged to protect competitive advantage while enabling incremental software-enabled improvements that can be deployed under existing regulatory clearances.
Competitive positioning increasingly hinges on ecosystem orchestration rather than single-product superiority. Firms that can align clinical workflow support, training services, and outcome-tracking tools alongside their devices create stronger switching costs for customers. At the same time, smaller innovators are attracting attention through targeted niche solutions-such as capsule platforms for specific gastrointestinal indications or highly flexible tools tailored for bronchial navigation-creating a bifurcated competitive environment where scale and specialization coexist. Investors and corporate development teams are therefore prioritizing opportunities that offer either clear path to scale or defensible specialization backed by clinical differentiation.
Actionable, prioritized recommendations for leaders to strengthen supply chains, accelerate clinical validation, and optimize commercial models for scalable adoption
Industry leaders should prioritize a dual-track strategy that balances near-term operational resilience with longer-term platform differentiation. In the near term, companies should secure supply chain flexibility by diversifying qualified suppliers, enhancing bill-of-materials traceability, and pursuing tariff mitigation strategies where appropriate. Concurrently, focus on modularity in hardware and software will enable faster iteration cycles and reduce the cost of compliance for incremental improvements. Investing in robust clinical evidence programs that demonstrate procedure-level benefits and patient-centered outcomes will accelerate reimbursement dialogues and reduce purchaser risk aversion.
Commercially, firms should tailor go-to-market approaches to the specific needs of hospitals, ambulatory centers, and clinics, aligning direct sales efforts with high-touch clinical training and channel partnerships for broad geographic coverage. Strategic partnerships with imaging and software vendors can create bundled value propositions that are harder to replicate. Finally, leadership teams should consider alternative commercial constructs such as managed equipment services, outcome-based pricing pilots, and subscription models for analytics to unlock new adoption vectors and smoother revenue streams. Executed together, these moves will strengthen resilience and position companies to benefit from the structural changes reshaping endoscopy care delivery.
A transparent description of the mixed-methods research approach used to compile evidence, validate themes, and ensure practical relevance for decision-makers
The research underpinning this executive analysis combined primary and secondary methods to ensure rigorous, multi-dimensional validation of insights. Primary research included structured interviews with clinical leaders, procurement specialists, and senior executives involved in product strategy, along with observational reviews of procedural workflows where available. Secondary research encompassed peer-reviewed clinical literature, regulatory filings, patent records, and manufacturer technical documentation to triangulate technology trends and device capabilities.
Synthesis processes involved cross-validation of qualitative insights with document-based evidence, thematic coding of interview transcripts to identify recurring operational challenges and innovation priorities, and mapping of regulatory milestones against product introductions. The methodology acknowledges inherent limitations, including variability in clinical practice across regions and uneven public disclosure of proprietary cost structures. To mitigate these constraints, findings were stress-tested with multiple stakeholders and framed conservatively to reflect practice realities rather than vendor claims. The resulting approach balances depth of technical understanding with pragmatic relevance for decision-makers.
A succinct conclusion that synthesizes strategic priorities and clarifies the organizational capabilities needed to capture value from advancements in robotic endoscopy
The robotic endoscopy device landscape is at a strategic inflection point where technological capability, clinical evidence, and commercial model innovation converge to create new opportunities and operational challenges. Advances in capsule, flexible, and rigid robotic platforms are enabling clinicians to reconsider procedural boundaries, while regulatory and procurement dynamics are shaping how and where these technologies scale. Supply chain pressures, including trade measures and component sourcing complexity, are forcing companies to adapt their manufacturing logic and design priorities to preserve competitiveness.
For stakeholders considering engagement-whether through procurement, partnership, investment, or clinical adoption-the imperative is to evaluate opportunities through a multi-dimensional lens that integrates clinical outcomes, economic implications, and operational feasibility. Organizations that align product roadmaps with pragmatic regulatory strategies, resilient supply chains, and targeted evidence generation will be best positioned to translate innovation into sustainable clinical impact and commercial success. The most successful entrants will be those that treat robotic endoscopy not as an isolated product play but as a systems-level offering that must harmonize technology, clinical workflows, and service delivery.
Please Note: PDF & Excel + Online Access - 1 Year
Table of Contents
180 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 AI-driven computer vision and force feedback in robotic endoscopy platforms
- 5.2. Development of magnetically actuated capsule endoscopes for targeted colon screening procedures
- 5.3. Expansion of single-use robotic endoscopes to mitigate infection risks in endoscopic procedures
- 5.4. Adoption of remote telesurgery platforms for robotic endoscopy with real-time physician guidance
- 5.5. Regulatory pathways accelerating approval of disposable robotic gastroscopes and colonoscopes
- 5.6. Emergence of AI-based polyp detection algorithms integrated into robotic endoscopy systems
- 5.7. Incorporation of advanced shape-sensing fiber optics for enhanced navigation in tortuous anatomy
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Robotic Endoscopy Devices Market, by Device Type
- 8.1. Diagnostic
- 8.1.1. Biopsy
- 8.1.2. Imaging
- 8.2. Therapeutic
- 8.2.1. Ablation
- 8.2.2. Hemostasis
- 8.2.3. Resection
- 9. Robotic Endoscopy Devices Market, by Technology
- 9.1. Capsule Endoscope
- 9.2. Flexible Robotic Endoscope
- 9.3. Rigid Robotic Endoscope
- 10. Robotic Endoscopy Devices Market, by Application
- 10.1. Bronchial
- 10.2. Gastrointestinal
- 10.2.1. Lower Gastrointestinal
- 10.2.2. Upper Gastrointestinal
- 10.3. Otolaryngological
- 10.4. Urological
- 11. Robotic Endoscopy Devices Market, by End User
- 11.1. Ambulatory Surgical Centers
- 11.2. Clinics
- 11.3. Hospitals
- 11.4. Research Institutes
- 12. Robotic Endoscopy Devices 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. Robotic Endoscopy Devices Market, by Group
- 13.1. ASEAN
- 13.2. GCC
- 13.3. European Union
- 13.4. BRICS
- 13.5. G7
- 13.6. NATO
- 14. Robotic Endoscopy Devices 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. Ambu A/S
- 15.3.2. Asensus Surgical, Inc.
- 15.3.3. avateramedical GmbH
- 15.3.4. Boston Scientific Corporation
- 15.3.5. Brainlab AG
- 15.3.6. CMR Surgical Ltd.
- 15.3.7. Cook Group Incorporated
- 15.3.8. EndoMaster Pte Ltd
- 15.3.9. Endotics
- 15.3.10. Globus Medical, Inc.
- 15.3.11. Intuitive Surgical, Inc.
- 15.3.12. KARL STORZ SE & Co. KG
- 15.3.13. Medtronic PLC
- 15.3.14. MicroPort Scientific Corporation
- 15.3.15. Olympus Corporation
- 15.3.16. Otsuka Holdings Co., Ltd.
- 15.3.17. Renishaw PLC
- 15.3.18. Ronovo Surgical
- 15.3.19. Stryker Corporation
- 15.3.20. Virtuoso Surgical, Inc.
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