내시경 초음파 시장 : 제품, 용도, 기술, 최종사용자별 - 세계 예측(2025-2032년)

The Endoscopy Ultrasound Market is projected to grow by USD 2.08 billion at a CAGR of 7.99% by 2032.

A concise orienting overview of how technological innovation and clinical practice evolution are redefining the role of endoscopic ultrasound in contemporary gastrointestinal and pancreatobiliary care

Endoscopic ultrasound (EUS) has evolved into a pivotal modality that bridges endoscopy and cross-sectional imaging to provide high-resolution visualization and tissue characterization in complex gastrointestinal and pancreatobiliary disease. Recent advances in probe designs, imaging physics, and adjunctive technologies have expanded indications, improved diagnostic yield, and created new interventional opportunities while reshaping multidisciplinary care pathways. As the procedural landscape shifts toward minimally invasive diagnostics and therapeutics, EUS plays an increasingly central role in staging, targeted biopsy, and guided interventions that reduce time to diagnosis and enable downstream personalized treatment planning.

Clinical adoption is being driven not only by improvements in image quality and accessory compatibility but also by heightened clinician experience and evolving training paradigms. Concurrently, device manufacturers are investing in ergonomics, probe versatility, and integrated imaging suites that support real-time decision-making. Regulatory frameworks and reimbursement policies are adapting to these clinical advances, influencing deployment priorities in hospitals, diagnostic centers, and ambulatory surgery settings. Taken together, these dynamics set the stage for a period of technology-driven clinical maturation in which EUS becomes more deeply embedded in standard diagnostic algorithms and interventional toolkits.

How probe innovation, software-enabled imaging, and workflow integration are collectively transforming endoscopic ultrasound from a diagnostic adjunct into a procedural mainstay

The EUS landscape is undergoing transformative shifts driven by improvements in probe architectures, software-enabled image enhancement, and the migration of interventional capabilities from open surgical suites into endoscopy suites. Advances in forward viewing, linear array, and radial array probe designs have expanded procedural versatility, enabling clinicians to select devices that optimize field of view, needle trajectory, and access for specific clinical tasks. Simultaneously, imaging enhancements such as contrast enhancement and elastography, along with the emergence of three-dimensional reconstruction techniques and mini probes, are enhancing lesion characterization and procedural confidence.

Integration of digital workflows and compatibility with ancillary devices is accelerating the translation of EUS into complex interventions, including targeted biopsies, drainage procedures, and tumor-directed therapies. Training programs and simulation technologies are evolving in parallel to reduce the learning curve and promote safer adoption of therapeutic applications. Health systems are responding by creating multidisciplinary pathways that incorporate EUS outcomes into tumor boards and care coordination. These shifts collectively signal a move from diagnostic adjunct to procedural mainstay, driven by patient-centered demands for less invasive, higher-precision care.

Assessing the operational and procurement impacts of the United States tariff adjustments in 2025 on device sourcing, supplier strategies, and clinical availability for endoscopic ultrasound

Tariff changes and trade policy adjustments can create ripple effects across supply chains, procurement decisions, and device lifecycles within the healthcare sector. In the United States specifically, revised tariff schedules implemented in 2025 have altered landed costs for certain medical devices and components, prompting procurement teams and manufacturers to reassess sourcing strategies and contract terms. When import duties increase, manufacturers and distributors evaluate domestic production options, regional logistics strategies, and long-term supplier commitments to preserve margins and maintain supply continuity.

Procurement teams are responding by intensifying supplier diversification, seeking closer collaboration on total landed cost visibility, and exploring consignment or risk-sharing agreements to mitigate short-term price volatility. Clinical programs are increasingly focused on articulating value through outcomes and efficiencies to justify procurement choices to hospital finance and supply chain committees. Meanwhile, device developers are accelerating design-for-manufacture initiatives and localization strategies to reduce exposure to tariff-driven cost increases and to enhance control over quality and delivery timelines. These adaptive measures aim to sustain device availability for critical diagnostic and interventional procedures despite trade-related headwinds.

Integrated segmentation perspectives revealing how product typologies, clinical indications, imaging technologies, and care settings jointly influence device selection and clinical utilization

Segmentation analysis illuminates how product, application, technology, and end-user dynamics interact to shape clinical adoption and purchasing preferences. When examining products across forward viewing, linear array, and radial array probe types, clinical teams prioritize device attributes tied to the procedural portfolio: forward viewing probes are valued for direct therapeutic access, linear arrays for needle-guided interventions and sampling precision, and radial arrays for circumferential anatomic surveys and initial diagnostic orientation. Clinicians and procurement professionals often balance these differences against procedural volumes and specialty mix when selecting a probe set for an institution.

Application-driven segmentation underscores differing clinical evidence needs across gastrointestinal tumors, lymph node staging, pancreatobiliary diseases, and submucosal tumors. For each application, diagnostic sensitivity, safe therapeutic access, and integration with multidisciplinary care pathways determine clinical value. Technology segmentation reveals nuanced adoption patterns for contrast enhancement, elastography, mini probes, and three-dimensional EUS, with contrast enhancement evaluated both at the agent level and through parameter quantification, and elastography adoption influenced by distinctions between shear wave and strain techniques. Three-dimensional EUS shows divergent clinical utility depending on whether offline reconstruction or real-time three-dimensional capability is available. Finally, end-user segmentation across ambulatory surgery centers, diagnostic centers, and hospitals highlights divergent capital investment profiles, procedural throughput expectations, and staffing models that drive which device configurations and service offerings are most practical for each care setting.

How regional regulatory environments, reimbursement frameworks, and infrastructure investments across the Americas, Europe Middle East & Africa, and Asia-Pacific shape adoption and deployment strategies for advanced EUS technologies

Regional dynamics continue to shape adoption trajectories and investment priorities across the Americas, Europe Middle East & Africa, and Asia-Pacific, with each geography presenting distinct clinical drivers, regulatory pathways, and procurement ecosystems. In the Americas, institutional procurement tends to emphasize integrated service support, bundled maintenance agreements, and evidence demonstrating procedural efficiency and clinical outcomes, prompting systems to prioritize devices that align with high-volume tertiary care and complex interventional programs. Payment models and clinical guideline uptake influence how innovations are prioritized and scaled.

Across Europe, the Middle East, and Africa, regulatory harmonization efforts, reimbursement variability, and infrastructure heterogeneity create a landscape in which device manufacturers must offer flexible commercial models and robust post-market data to support adoption in diverse settings. Capacity building and training partnerships can be particularly influential in expanding advanced applications beyond major urban centers. In the Asia-Pacific region, rapid investments in hospital infrastructure, increasing specialist capacity, and a strong emphasis on minimally invasive care accelerate uptake of advanced imaging adjuncts and therapeutic EUS procedures. Regional supply chain considerations, distribution networks, and localized service capabilities further determine how quickly new technologies are translated into routine clinical practice.

Competitive dynamics driven by product portfolio depth, clinical partnerships, and aftermarket service models that determine perceived value and procurement decisions in EUS

Competitive dynamics in the EUS ecosystem are influenced by a combination of product depth, clinical evidence, aftermarket services, and collaborative clinical partnerships. Established manufacturers with broad device portfolios often differentiate through comprehensive service offerings, integrated imaging platforms, and existing relationships with large hospital systems. At the same time, innovative entrants focus on modular designs, niche imaging modalities, and targeted therapeutic solutions that address specific clinical gaps, creating a complementary competitive set rather than a zero-sum environment.

Strategic alliances between device developers, imaging software providers, and clinical centers of excellence are accelerating evidence generation and shaping perceived value. Manufacturers that invest in clinician training, simulation, and procedural workflow optimization can accelerate adoption by reducing implementation friction. Moreover, aftermarket considerations such as warranty structures, consumable compatibility, and remote diagnostics increasingly inform procurement decisions, as health systems weigh the total cost of ownership against clinical performance and operational resilience.

Practical strategic actions for device teams and clinical leaders to align procurement, training, and interoperability priorities for successful EUS program expansion

Leaders in device development, hospital procurement, and clinical program management should pursue a set of coordinated, actionable approaches to convert insights into measurable outcomes. First, align device selection with procedural portfolios and training capacity to ensure that investments deliver clinical flexibility and incremental therapeutic capability. When procurement teams and clinical leadership co-design equipment specifications and support contracts, institutions can better balance capital commitments with utilization goals.

Second, prioritize interoperability and software-enabled workflow features that reduce procedure time and enhance diagnostic confidence, while investing in clinician training and simulation to shorten adoption curves. Third, develop supplier engagement strategies that incorporate risk-sharing on consumables, service-level guarantees, and local spare-part inventories to mitigate supply chain volatility. Fourth, invest in post-procedural outcome tracking that links EUS-derived diagnoses and interventions to downstream care pathways, enabling clearer value articulation to payers and institutional stakeholders. Collectively, these actions will help organizations capture clinical and operational benefits while managing cost and implementation risk.

A transparent and triangulated research approach combining practitioner interviews, clinical literature review, regulatory analysis, and supply chain assessment to ensure robust, evidence-based conclusions

The research methodology underpinning this report combined qualitative and quantitative methods to generate a comprehensive view of clinical practice, technology trends, and commercial dynamics. Primary research included structured interviews with practicing endoscopists, interventional gastroenterologists, procurement specialists, and clinical engineers to capture firsthand perspectives on device performance, training needs, and implementation challenges. Secondary sources encompassed peer-reviewed clinical literature, regulatory filings, product specifications, and publicly available clinical guidelines to corroborate practitioner insights and to map technology maturation pathways.

Analytical processes emphasized triangulation to validate findings across multiple data points, with attention to differentiation among product types, clinical indications, imaging modalities, and end-user environments. Supply chain analysis integrated trade policy changes and distribution architectures to assess operational risk. Case studies and representative clinical scenarios were employed to illustrate real-world implications of technology choices and workflow adaptations. Throughout, methodological rigor was maintained by documenting interview protocols, inclusion criteria for secondary sources, and the analytical frameworks used to synthesize evidence into actionable insights.

Synthesis of clinical, technological, and operational trajectories that policymakers, clinicians, and procurement leaders should consider when accelerating responsible adoption of advanced EUS capabilities

In closing, endoscopic ultrasound stands at an inflection point where technological maturation, clinical demand for less invasive diagnostics, and evolving procurement environments converge to expand its clinical footprint. Advancements in probe design, contrast and elastography techniques, and three-dimensional imaging are enhancing diagnostic precision and enabling more complex interventions to be performed safely within endoscopy suites. As institutions and device developers adapt to supply chain and policy shifts, coordinated investments in training, interoperability, and supplier relationships will be critical to sustaining adoption.

Decision-makers should treat these developments as an opportunity to modernize procedural pathways, strengthen multidisciplinary collaboration, and invest in outcome measurement to demonstrate value. By doing so, clinical programs can better position themselves to deliver high-quality, efficient care while navigating commercial and operational complexities. The insights compiled here provide a practical foundation for clinicians, procurement leaders, and device developers to refine strategy and accelerate responsible adoption of advanced EUS capabilities.

Table of Contents

1. Preface

• 1.1. Objectives of the Study
• 1.2. Market Segmentation & Coverage
• 1.3. Years Considered for the Study
• 1.4. Currency & Pricing
• 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 in endoscopic ultrasound for real-time lesion characterization
• 5.2. Adoption of high-frequency catheter probes to enhance resolution in vascular and biliary tract imaging using endoscopic ultrasound
• 5.3. Development of miniaturized forward-viewing ultrasound transducers for endoscopic access to complex gastrointestinal anatomy
• 5.4. Implementation of elastography techniques in endoscopic ultrasound for noninvasive assessment of tissue stiffness and fibrosis
• 5.5. Emergence of contrast-enhanced endoscopic ultrasound to improve diagnostic accuracy in pancreatic lesion evaluation
• 5.6. Integration of telehealth connectivity features in endoscopic ultrasound platforms for remote expert consultation and training
• 5.7. Introduction of single-use disposable endoscopic ultrasound accessories to reduce cross-contamination risks and streamline workflows
• 5.8. Advances in 3D and 4D reconstruction software for endoscopic ultrasound to enhance spatial visualization of complex lesions
• 5.9. Rising collaboration between endoscopic ultrasound device manufacturers and pharmaceutical companies for targeted drug delivery studies
• 5.10. Regulatory approval of novel endoscopic ultrasound-guided ablation technologies for minimally invasive treatment of gastrointestinal tumors

6. Cumulative Impact of United States Tariffs 2025

7. Cumulative Impact of Artificial Intelligence 2025

8. Endoscopy Ultrasound Market, by Product

• 8.1. Forward Viewing
• 8.2. Linear Array
• 8.3. Radial Array

9. Endoscopy Ultrasound Market, by Application

• 9.1. Gastrointestinal Tumors
• 9.2. Lymph Node Staging
• 9.3. Pancreatobiliary Diseases
• 9.4. Submucosal Tumors

10. Endoscopy Ultrasound Market, by Technology

• 10.1. Contrast Enhancement
  • 10.1.1. Microbubble Agents
  • 10.1.2. Parameter Quantification
• 10.2. Elastography
  • 10.2.1. Shear Wave
  • 10.2.2. Strain
• 10.3. Mini Probes
• 10.4. Three D EUS
  • 10.4.1. Offline Reconstruction
  • 10.4.2. Real Time Three D

11. Endoscopy Ultrasound Market, by End User

• 11.1. Ambulatory Surgery Centers
• 11.2. Diagnostic Centers
• 11.3. Hospitals

12. Endoscopy Ultrasound 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 Ultrasound Market, by Group

• 13.1. ASEAN
• 13.2. GCC
• 13.3. European Union
• 13.4. BRICS
• 13.5. G7
• 13.6. NATO

14. Endoscopy Ultrasound 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. FUJIFILM Holdings Corporation
  • 15.3.3. HOYA Corporation
  • 15.3.4. Boston Scientific Corporation
  • 15.3.5. Medtronic plc
  • 15.3.6. Koninklijke Philips N.V.
  • 15.3.7. Canon Medical Systems Corporation
  • 15.3.8. Siemens Healthineers AG
  • 15.3.9. General Electric Company
  • 15.3.10. Hitachi, Ltd.