Surgical Robots Market by Component (Instruments & Accessories, Robotic Systems, Software & Services), Type (General Surgery Robots, Laparoscopic Robots, Neurosurgical Robots), Technology, End User - Global Forecast 2025-2032
Description
The Surgical Robots Market was valued at USD 9.30 billion in 2024 and is projected to grow to USD 10.08 billion in 2025, with a CAGR of 9.60%, reaching USD 19.38 billion by 2032.
A concise framing of the surgical robotics environment highlighting technological convergence, clinical demands, and operational decision points for strategic leaders
The landscape of surgical robotics is evolving at a rapid and systemic pace, driven by converging advances in robotics, imaging, artificial intelligence, and health systems policy. Hospitals and specialty providers are integrating robotic capabilities across a widening set of procedures, seeking predictable outcomes, reduced variability, and operational efficiencies. At the same time, software and services are moving from adjunct roles to central enablers of perioperative planning, intraoperative guidance, and postoperative analytics, reshaping how care teams coordinate and measure clinical performance.
Against this backdrop, stakeholders face a complex interplay of clinical evidence requirements, capital allocation decisions, and supply chain considerations. Clinical leaders demand robust evidence of value beyond single-center experiences, while procurement functions weigh total cost of ownership, training burdens, and interoperability. Innovators must therefore balance incremental hardware improvements with software-driven workflow gains, partnering with clinicians and health systems to validate outcomes and to scale adoption across diverse care settings. This executive summary synthesizes key shifts, segmentation insights, regional dynamics, competitive developments, and pragmatic recommendations designed to inform strategic choices in this dynamic environment.
An integrated view of how modular hardware, software-centric value, evolving procurement models, and modern workforce training are reshaping clinical adoption
Over the past several years, transformative shifts have redefined both the promise and the practicalities of robotic-assisted surgery, altering the calculus for clinicians, hospital executives, and device developers. First, the transition from single-procedure platforms to multi-quadrant, modular systems has extended robotic applicability across general surgery, urology, orthopedics, and neurosurgery. This shift is accompanied by improved ergonomics, reusable instrument strategies, and integrated imaging that collectively reduce procedure time variability and expand surgeon acceptance.
Second, the emergence of software-centric value propositions is changing commercial models. Artificial intelligence-enabled planning, closed-loop control for precision tasks, and cloud-based analytics have made software and services indispensable complements to hardware, enabling continuous performance improvement and remote proctoring. Third, procurement and contracting practices are evolving: hospitals increasingly seek outcome-linked procurement, bundled service agreements, and managed-service approaches that align vendor incentives with procedural quality. Finally, workforce and training models are adapting; virtual reality simulation, telementoring, and competency-based credentialing are enabling more rapid, standardized skill diffusion across heterogeneous clinical settings. Collectively, these shifts are creating a more interconnected, software-enabled, and outcome-focused surgical robotics ecosystem.
How evolving tariff dynamics influence supply chains, sourcing strategies, and procurement timelines across surgical robotics value chains
Policy instruments such as tariffs and trade measures are exerting a measurable influence on the global supply chain for surgical robotics and related components. Tariff-driven cost pressures can increase the landed cost of key subsystems, including precision instruments, actuators, and imaging modules, which in turn influences sourcing decisions, inventory strategies, and supplier diversification efforts. Import duties can also affect the timing of capital deployments, as procurement cycles may be delayed pending clarity on regulatory or tariff adjustments, leading health systems to reassess trade-offs between upgrading legacy systems and investing in next-generation platforms.
Beyond direct cost impacts, tariffs can catalyze strategic adjustments across the value chain. Some suppliers respond by re-shoring or near-shoring assemblies to reduce exposure to trade disruptions, which can improve lead times but may require new capital investments and regulatory approvals. Others deepen partnerships with regional contract manufacturers to mitigate customs risk. In addition, tariffs can affect aftermarket dynamics; elevated costs of replacement instruments or proprietary consumables may accelerate customer interest in reusable solutions or open-platform interoperability. Regulators and hospital procurement teams are increasingly evaluating total lifecycle resilience, and smart manufacturers are building multi-origin sourcing and transparent cost models to maintain competitive positioning despite policy volatility.
High-resolution segmentation insights that explain component-, type-, technology-, and end-user-specific adoption dynamics and commercialization levers
Segmentation-driven insights reveal differentiated value drivers and adoption barriers across components, types, technologies, and end users, providing a nuanced basis for commercial prioritization. When analyzed by component, the industry displays distinct dynamics between Instruments & Accessories, Robotic Systems, and Software & Services: instruments and accessories face recurring consumable cost scrutiny and sterilization workflow demands, robotic systems require capital justification and integration with operating room infrastructure, while software and services increasingly drive differentiation through analytics, cloud connectivity, and workflow optimization.
By type, adoption patterns vary across General Surgery Robots, Laparoscopic Robots, Neurosurgical Robots, Orthopedic Robots, and Urological Robots, each presenting unique clinical evidence requirements, capital intensity, and training pathways. Neurosurgical and orthopedic applications often demand ultra-high accuracy and integration with advanced imaging, whereas urological and laparoscopic deployments emphasize procedural throughput and ergonomics. Technology choices also matter: Telerobotic architectures enable remote collaboration and proctoring but require robust connectivity and cybersecurity measures, while Tethered or Console-Based Robots prioritize low-latency tactile feedback and established operating room integrations. Finally, end-user distinctions-Ambulatory Surgical Centers, Hospitals, Research Institutes, and Specialty Clinics-shape purchasing rationales and service needs; ambulatory centers prioritize throughput and cost per case, hospitals balance inpatient complexity and multi-specialty utility, research institutes focus on experimental flexibility and integration with investigational devices, and specialty clinics emphasize procedure-specific ROI and patient experience enhancements. These segmentation lenses together provide a practical roadmap for prioritizing investments, tailoring commercial models, and designing evidence-generation strategies that resonate with specific customer cohorts.
Regional dynamics and procurement realities across Americas, Europe Middle East & Africa, and Asia-Pacific that shape adoption, procurement, and local innovation
Regional dynamics influence clinical priorities, reimbursement pathways, manufacturing footprints, and collaborative innovation networks, producing differentiated adoption curves across geographies. In the Americas, health systems demonstrate strong interest in procedural standardization, bundled payment models, and data-driven quality programs; these forces favor platforms that can demonstrate consistent outcomes, integrate with electronic health records, and enable cross-facility benchmarking. The Americas also host significant clinical trial activity and procurements driven by system-level strategies to differentiate on surgical quality.
Across Europe, Middle East & Africa, regulatory harmonization, centralized purchasing mechanisms in some countries, and a growing emphasis on value-based procurement guide adoption patterns, with health ministries and large hospital networks often seeking scalable solutions that balance capital costs and long-term service models. In the Asia-Pacific region, rapid infrastructure expansion, growing surgical volumes, and a strong focus on cost-efficiency are encouraging innovative financing arrangements and partnerships with local manufacturers. Additionally, Asia-Pacific is a fertile ground for clinical innovation and diversified manufacturing ecosystems, which can accelerate iterative design and regional customization. Overall, regional strategies must be tailored to local reimbursement, procurement norms, and clinical ecosystem maturity in order to succeed.
Competitive landscape insights showing how incumbents, specialists, and software players are forging alliances, service models, and differentiation strategies
Competitive dynamics in surgical robotics are defined by a mix of large medtech incumbents, specialized robotics innovators, and software-centric entrants, each pursuing distinct routes to scale. Established device manufacturers leverage installed bases, clinical relationships, and broad capital equipment portfolios to offer integrated solutions and bundled service agreements. They typically focus on enhancing system versatility, reducing per-procedure costs through longer-lifecycle instruments, and strengthening service networks to minimize downtime.
At the same time, focused robotics companies and start-ups are differentiating through single-procedure optimization, modular architectures, and novel control modalities that promise workflow simplification and specialized clinical benefits. Software-first companies are increasingly important, offering perioperative planning, intraoperative guidance, and post-procedure analytics that can be layered onto multiple hardware platforms. Partnerships and strategic alliances between hardware vendors and software providers are accelerating, as companies recognize the commercial necessity of interoperable ecosystems. Service models are also evolving, with subscription-based access, managed services, and outcome-linked contracts gaining traction as ways to align vendor incentives with health system goals. Competitive advantage will accrue to organizations that couple clinical validation with clear total lifecycle value propositions and flexible commercial terms.
Practical strategic priorities for clinical validation, flexible commercial models, resilient supply chains, and scalable workforce enablement to accelerate adoption
Industry leaders should pursue a coordinated set of strategic actions that address clinical credibility, operational integration, and supply-chain resilience. First, prioritize rigorous clinical evidence generation tied to meaningful patient-centered outcomes and healthcare economics; prospective, multicenter studies and real-world evidence initiatives will accelerate payer and provider acceptance. Second, design commercial models that reduce adoption friction by aligning vendor revenue with client outcomes, offering flexible financing, managed-service options, and modular upgrade paths that lower upfront barriers.
Third, invest in software platforms that enable interoperability, analytics, and remote support, thereby turning hardware into an extensible service offering and deepening customer lock-in. Fourth, build resilient supply chains through multi-origin sourcing, regional manufacturing partnerships, and transparent aftermarket strategies to mitigate tariff and logistics risks. Fifth, scale workforce enablement by developing standardized training curricula, validated simulation programs, and competency-based credentialing to reduce variability in clinical performance. Finally, pursue collaborative regulatory and reimbursement engagement with policymakers and payers to clarify pathways for approval and value recognition. Taken together, these actions create a defensible commercial position and accelerate sustainable adoption across diverse care settings.
A transparent, mixed-methods research process combining stakeholder interviews, technical review, and supply chain and policy analysis to validate findings
The research approach combined qualitative and quantitative techniques to ensure robust, triangulated findings and high confidence in thematic conclusions. Primary research included structured interviews with surgeons, hospital procurement executives, biomedical engineers, and clinical operations leaders to capture real-world adoption drivers, barriers, and performance expectations. These interviews were complemented by case study analyses of early adopter institutions and technology deployments to understand integration challenges, training pathways, and outcomes measurement practices.
Secondary research involved systematic reviews of peer-reviewed clinical literature, regulatory filings, technical specifications, patents, and industry reports to map technology trajectories and competitive positioning. Supply chain and policy analyses incorporated customs and trade documentation, logistics reports, and public policy announcements to assess exposure to tariff-related dynamics. Data validation and synthesis were conducted through iterative cross-checking between primary insights and secondary evidence, followed by expert panel reviews to surface alternative interpretations and to stress-test recommendations. Throughout the process, emphasis was placed on transparency of assumptions, reproducibility of methods, and alignment of evidence with actionable business implications.
Synthesis of strategic imperatives where technology maturation, evidence generation, and operational resilience converge to determine long-term competitive outcomes
The cumulative picture is one of an industry at the intersection of technological maturation and commercial recalibration, where clinical evidence, software-enabled value, and resilient operational strategies will determine winners and followers. Surgical robotics is transitioning from niche, procedure-specific deployments to an ecosystem where interoperability, outcome measurement, and scalable service models matter as much as hardware performance. Strategic decisions made now about partnerships, evidence generation, and supply-chain structure will have lasting implications for adoption trajectories and competitive positioning.
Leaders should therefore act deliberately to align product roadmaps with clinical workflows, invest in interoperable software and data capabilities, and build flexible commercial offers that lower barriers to adoption. Simultaneously, proactive supply-chain planning and regional manufacturing strategies will mitigate policy risk and improve responsiveness. By balancing near-term commercialization with sustained investments in clinical validation and customer training, organizations can capture value from the ongoing transformation of surgical care delivery while managing operational and policy headwinds.
Please Note: PDF & Excel + Online Access - 1 Year
A concise framing of the surgical robotics environment highlighting technological convergence, clinical demands, and operational decision points for strategic leaders
The landscape of surgical robotics is evolving at a rapid and systemic pace, driven by converging advances in robotics, imaging, artificial intelligence, and health systems policy. Hospitals and specialty providers are integrating robotic capabilities across a widening set of procedures, seeking predictable outcomes, reduced variability, and operational efficiencies. At the same time, software and services are moving from adjunct roles to central enablers of perioperative planning, intraoperative guidance, and postoperative analytics, reshaping how care teams coordinate and measure clinical performance.
Against this backdrop, stakeholders face a complex interplay of clinical evidence requirements, capital allocation decisions, and supply chain considerations. Clinical leaders demand robust evidence of value beyond single-center experiences, while procurement functions weigh total cost of ownership, training burdens, and interoperability. Innovators must therefore balance incremental hardware improvements with software-driven workflow gains, partnering with clinicians and health systems to validate outcomes and to scale adoption across diverse care settings. This executive summary synthesizes key shifts, segmentation insights, regional dynamics, competitive developments, and pragmatic recommendations designed to inform strategic choices in this dynamic environment.
An integrated view of how modular hardware, software-centric value, evolving procurement models, and modern workforce training are reshaping clinical adoption
Over the past several years, transformative shifts have redefined both the promise and the practicalities of robotic-assisted surgery, altering the calculus for clinicians, hospital executives, and device developers. First, the transition from single-procedure platforms to multi-quadrant, modular systems has extended robotic applicability across general surgery, urology, orthopedics, and neurosurgery. This shift is accompanied by improved ergonomics, reusable instrument strategies, and integrated imaging that collectively reduce procedure time variability and expand surgeon acceptance.
Second, the emergence of software-centric value propositions is changing commercial models. Artificial intelligence-enabled planning, closed-loop control for precision tasks, and cloud-based analytics have made software and services indispensable complements to hardware, enabling continuous performance improvement and remote proctoring. Third, procurement and contracting practices are evolving: hospitals increasingly seek outcome-linked procurement, bundled service agreements, and managed-service approaches that align vendor incentives with procedural quality. Finally, workforce and training models are adapting; virtual reality simulation, telementoring, and competency-based credentialing are enabling more rapid, standardized skill diffusion across heterogeneous clinical settings. Collectively, these shifts are creating a more interconnected, software-enabled, and outcome-focused surgical robotics ecosystem.
How evolving tariff dynamics influence supply chains, sourcing strategies, and procurement timelines across surgical robotics value chains
Policy instruments such as tariffs and trade measures are exerting a measurable influence on the global supply chain for surgical robotics and related components. Tariff-driven cost pressures can increase the landed cost of key subsystems, including precision instruments, actuators, and imaging modules, which in turn influences sourcing decisions, inventory strategies, and supplier diversification efforts. Import duties can also affect the timing of capital deployments, as procurement cycles may be delayed pending clarity on regulatory or tariff adjustments, leading health systems to reassess trade-offs between upgrading legacy systems and investing in next-generation platforms.
Beyond direct cost impacts, tariffs can catalyze strategic adjustments across the value chain. Some suppliers respond by re-shoring or near-shoring assemblies to reduce exposure to trade disruptions, which can improve lead times but may require new capital investments and regulatory approvals. Others deepen partnerships with regional contract manufacturers to mitigate customs risk. In addition, tariffs can affect aftermarket dynamics; elevated costs of replacement instruments or proprietary consumables may accelerate customer interest in reusable solutions or open-platform interoperability. Regulators and hospital procurement teams are increasingly evaluating total lifecycle resilience, and smart manufacturers are building multi-origin sourcing and transparent cost models to maintain competitive positioning despite policy volatility.
High-resolution segmentation insights that explain component-, type-, technology-, and end-user-specific adoption dynamics and commercialization levers
Segmentation-driven insights reveal differentiated value drivers and adoption barriers across components, types, technologies, and end users, providing a nuanced basis for commercial prioritization. When analyzed by component, the industry displays distinct dynamics between Instruments & Accessories, Robotic Systems, and Software & Services: instruments and accessories face recurring consumable cost scrutiny and sterilization workflow demands, robotic systems require capital justification and integration with operating room infrastructure, while software and services increasingly drive differentiation through analytics, cloud connectivity, and workflow optimization.
By type, adoption patterns vary across General Surgery Robots, Laparoscopic Robots, Neurosurgical Robots, Orthopedic Robots, and Urological Robots, each presenting unique clinical evidence requirements, capital intensity, and training pathways. Neurosurgical and orthopedic applications often demand ultra-high accuracy and integration with advanced imaging, whereas urological and laparoscopic deployments emphasize procedural throughput and ergonomics. Technology choices also matter: Telerobotic architectures enable remote collaboration and proctoring but require robust connectivity and cybersecurity measures, while Tethered or Console-Based Robots prioritize low-latency tactile feedback and established operating room integrations. Finally, end-user distinctions-Ambulatory Surgical Centers, Hospitals, Research Institutes, and Specialty Clinics-shape purchasing rationales and service needs; ambulatory centers prioritize throughput and cost per case, hospitals balance inpatient complexity and multi-specialty utility, research institutes focus on experimental flexibility and integration with investigational devices, and specialty clinics emphasize procedure-specific ROI and patient experience enhancements. These segmentation lenses together provide a practical roadmap for prioritizing investments, tailoring commercial models, and designing evidence-generation strategies that resonate with specific customer cohorts.
Regional dynamics and procurement realities across Americas, Europe Middle East & Africa, and Asia-Pacific that shape adoption, procurement, and local innovation
Regional dynamics influence clinical priorities, reimbursement pathways, manufacturing footprints, and collaborative innovation networks, producing differentiated adoption curves across geographies. In the Americas, health systems demonstrate strong interest in procedural standardization, bundled payment models, and data-driven quality programs; these forces favor platforms that can demonstrate consistent outcomes, integrate with electronic health records, and enable cross-facility benchmarking. The Americas also host significant clinical trial activity and procurements driven by system-level strategies to differentiate on surgical quality.
Across Europe, Middle East & Africa, regulatory harmonization, centralized purchasing mechanisms in some countries, and a growing emphasis on value-based procurement guide adoption patterns, with health ministries and large hospital networks often seeking scalable solutions that balance capital costs and long-term service models. In the Asia-Pacific region, rapid infrastructure expansion, growing surgical volumes, and a strong focus on cost-efficiency are encouraging innovative financing arrangements and partnerships with local manufacturers. Additionally, Asia-Pacific is a fertile ground for clinical innovation and diversified manufacturing ecosystems, which can accelerate iterative design and regional customization. Overall, regional strategies must be tailored to local reimbursement, procurement norms, and clinical ecosystem maturity in order to succeed.
Competitive landscape insights showing how incumbents, specialists, and software players are forging alliances, service models, and differentiation strategies
Competitive dynamics in surgical robotics are defined by a mix of large medtech incumbents, specialized robotics innovators, and software-centric entrants, each pursuing distinct routes to scale. Established device manufacturers leverage installed bases, clinical relationships, and broad capital equipment portfolios to offer integrated solutions and bundled service agreements. They typically focus on enhancing system versatility, reducing per-procedure costs through longer-lifecycle instruments, and strengthening service networks to minimize downtime.
At the same time, focused robotics companies and start-ups are differentiating through single-procedure optimization, modular architectures, and novel control modalities that promise workflow simplification and specialized clinical benefits. Software-first companies are increasingly important, offering perioperative planning, intraoperative guidance, and post-procedure analytics that can be layered onto multiple hardware platforms. Partnerships and strategic alliances between hardware vendors and software providers are accelerating, as companies recognize the commercial necessity of interoperable ecosystems. Service models are also evolving, with subscription-based access, managed services, and outcome-linked contracts gaining traction as ways to align vendor incentives with health system goals. Competitive advantage will accrue to organizations that couple clinical validation with clear total lifecycle value propositions and flexible commercial terms.
Practical strategic priorities for clinical validation, flexible commercial models, resilient supply chains, and scalable workforce enablement to accelerate adoption
Industry leaders should pursue a coordinated set of strategic actions that address clinical credibility, operational integration, and supply-chain resilience. First, prioritize rigorous clinical evidence generation tied to meaningful patient-centered outcomes and healthcare economics; prospective, multicenter studies and real-world evidence initiatives will accelerate payer and provider acceptance. Second, design commercial models that reduce adoption friction by aligning vendor revenue with client outcomes, offering flexible financing, managed-service options, and modular upgrade paths that lower upfront barriers.
Third, invest in software platforms that enable interoperability, analytics, and remote support, thereby turning hardware into an extensible service offering and deepening customer lock-in. Fourth, build resilient supply chains through multi-origin sourcing, regional manufacturing partnerships, and transparent aftermarket strategies to mitigate tariff and logistics risks. Fifth, scale workforce enablement by developing standardized training curricula, validated simulation programs, and competency-based credentialing to reduce variability in clinical performance. Finally, pursue collaborative regulatory and reimbursement engagement with policymakers and payers to clarify pathways for approval and value recognition. Taken together, these actions create a defensible commercial position and accelerate sustainable adoption across diverse care settings.
A transparent, mixed-methods research process combining stakeholder interviews, technical review, and supply chain and policy analysis to validate findings
The research approach combined qualitative and quantitative techniques to ensure robust, triangulated findings and high confidence in thematic conclusions. Primary research included structured interviews with surgeons, hospital procurement executives, biomedical engineers, and clinical operations leaders to capture real-world adoption drivers, barriers, and performance expectations. These interviews were complemented by case study analyses of early adopter institutions and technology deployments to understand integration challenges, training pathways, and outcomes measurement practices.
Secondary research involved systematic reviews of peer-reviewed clinical literature, regulatory filings, technical specifications, patents, and industry reports to map technology trajectories and competitive positioning. Supply chain and policy analyses incorporated customs and trade documentation, logistics reports, and public policy announcements to assess exposure to tariff-related dynamics. Data validation and synthesis were conducted through iterative cross-checking between primary insights and secondary evidence, followed by expert panel reviews to surface alternative interpretations and to stress-test recommendations. Throughout the process, emphasis was placed on transparency of assumptions, reproducibility of methods, and alignment of evidence with actionable business implications.
Synthesis of strategic imperatives where technology maturation, evidence generation, and operational resilience converge to determine long-term competitive outcomes
The cumulative picture is one of an industry at the intersection of technological maturation and commercial recalibration, where clinical evidence, software-enabled value, and resilient operational strategies will determine winners and followers. Surgical robotics is transitioning from niche, procedure-specific deployments to an ecosystem where interoperability, outcome measurement, and scalable service models matter as much as hardware performance. Strategic decisions made now about partnerships, evidence generation, and supply-chain structure will have lasting implications for adoption trajectories and competitive positioning.
Leaders should therefore act deliberately to align product roadmaps with clinical workflows, invest in interoperable software and data capabilities, and build flexible commercial offers that lower barriers to adoption. Simultaneously, proactive supply-chain planning and regional manufacturing strategies will mitigate policy risk and improve responsiveness. By balancing near-term commercialization with sustained investments in clinical validation and customer training, organizations can capture value from the ongoing transformation of surgical care delivery while managing operational and policy headwinds.
Please Note: PDF & Excel + Online Access - 1 Year
Table of Contents
190 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 algorithms for autonomous tissue identification during minimally invasive procedures
- 5.2. Development of haptic feedback enabled force sensing end effectors for delicate tissue manipulation
- 5.3. Miniaturized table top robotic platforms designed for point of care otolaryngology and neurosurgery applications
- 5.4. Expansion of remote telesurgery networks enabling real time surgeon to robot operations across continents
- 5.5. Integration of augmented reality three dimensional overlays for precision guidance in complex robotic procedures
- 5.6. Adoption of single port robotic systems optimized for scarless gynecologic and colorectal surgery interventions
- 5.7. Development of modular robotic arms with interchangeable instrument attachments for multi specialty hospitals
- 5.8. Emergence of cost effective disposable instrument sets aimed at reducing per procedure expenses in emerging markets
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Surgical Robots Market, by Component
- 8.1. Instruments & Accessories
- 8.2. Robotic Systems
- 8.3. Software & Services
- 9. Surgical Robots Market, by Type
- 9.1. General Surgery Robots
- 9.2. Laparoscopic Robots
- 9.3. Neurosurgical Robots
- 9.4. Orthopedic Robots
- 9.5. Urological Robots
- 10. Surgical Robots Market, by Technology
- 10.1. Telerobotic
- 10.2. Tethered / Console-Based Robots
- 11. Surgical Robots Market, by End User
- 11.1. Ambulatory Surgical Centers
- 11.2. Hospitals
- 11.3. Research Institutes
- 11.4. Specialty Clinics
- 12. Surgical Robots 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. Surgical Robots Market, by Group
- 13.1. ASEAN
- 13.2. GCC
- 13.3. European Union
- 13.4. BRICS
- 13.5. G7
- 13.6. NATO
- 14. Surgical Robots 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. Accuray Incorporated
- 15.3.2. AcuSurgical
- 15.3.3. Asensus Surgical US, Inc.
- 15.3.4. avateramedical GmbH
- 15.3.5. Brainlab AG
- 15.3.6. CMR Surgical Ltd.
- 15.3.7. Corin Group
- 15.3.8. Diligent Robotics Inc.
- 15.3.9. eCential Robotics
- 15.3.10. EndoQuest Robotics, Inc.
- 15.3.11. Globus Medical
- 15.3.12. Intuitive Surgical, Inc.
- 15.3.13. Johnson & Johnson Services. Inc.
- 15.3.14. KUKA AG by Midea Group
- 15.3.15. Medicaroid Corporation
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