영상 진단 장비 시장 : 제품 유형, 휴대성, 용도, 최종사용자별 - 세계 예측(2025-2032년)

The Diagnostic Imaging Equipment Market is projected to grow by USD 71.77 billion at a CAGR of 6.09% by 2032.

An authoritative overview of how technological innovation, clinical demand shifts, and operational imperatives are reshaping diagnostic imaging equipment adoption and use

Diagnostic imaging equipment continues to serve as the backbone of modern clinical decision-making, enabling earlier detection, more accurate diagnoses, and better treatment monitoring across a broad range of specialties. Imaging modalities such as computed tomography, magnetic resonance imaging, nuclear imaging, ultrasound, and X-ray remain integral to care pathways, while evolving clinical guidelines and technological advances are increasingly shaping procurement and utilization patterns. Stakeholders are navigating a complex environment where clinical efficacy, patient safety, cost containment, and workflow optimization must be balanced to deliver measurable value.

Clinical demands are being redefined by a confluence of demographic shifts and rising chronic disease prevalence, which together increase imaging volumes and place renewed emphasis on throughput and efficiency. At the same time, technological innovations-ranging from hardware miniaturization to software-driven image enhancement-are altering the value proposition of equipment investments. Providers and vendors must therefore consider not only capital cost but also lifecycle service models, integration with electronic health records, and the ability to support multidisciplinary care. Given this landscape, executives and clinical leaders need a clear, evidence-based picture of how modality-specific advances, regulatory changes, and reimbursement pressures will influence procurement strategies and operational priorities going forward.

How artificial intelligence, point-of-care modalities, hybrid imaging trends, and value-based imperatives are fundamentally altering the diagnostic imaging landscape

The diagnostic imaging landscape is undergoing fundamental transformation driven by converging technological, clinical, and economic forces. Artificial intelligence and advanced image analytics are enabling automated triage, enhanced lesion detection, and quantitative biomarkers that can accelerate diagnosis while improving reproducibility. Concurrently, hybrid imaging and multimodal integration are increasing clinical specificity by combining anatomical and functional data, which is transforming diagnostic algorithms in oncology and neurology.

Meanwhile, the push toward patient-centric care is promoting portable and point-of-care imaging solutions that decongest centralized radiology suites and bring diagnostic capability closer to bedside and community settings. Value-based reimbursement models are also reshaping purchase and service contracts, with providers placing greater emphasis on demonstrable outcomes, throughput, and total cost of ownership rather than acquisition price alone. Lastly, an increased focus on radiation dose optimization, environmental sustainability, and ergonomic design is influencing both product development and procurement criteria. As a result, companies that align product roadmaps with software-driven workflows, interoperability standards, and flexible commercial models are best positioned to capitalize on these transformative shifts.

Assessing how recent tariff shifts have reshaped supply chains, procurement decisions, and manufacturing strategies across the diagnostic imaging equipment value chain

The implementation of tariffs by the United States in 2025 introduced a new layer of complexity to global diagnostic imaging supply chains and procurement strategies. Manufacturers that relied on cross-border sourcing for precision components and semiconductor-dependent subsystems faced increased input costs and longer lead times, prompting rapid reassessment of supplier concentration risks. In response, many organizations accelerated efforts to diversify suppliers, nearshore production of critical subassemblies, and redesign products to reduce dependence on tariff-impacted parts.

Healthcare providers and equipment distributors experienced pressure to renegotiate purchase terms and service agreements, as cost pressures were often transferred through the supply chain. Capital expenditure committees became more sensitive to total lifecycle cost implications and to the balance between immediate capital outlay and long-term service commitments. At the same time, some vendors pursued vertical integration and strategic partnerships to secure critical inputs and stabilize pricing. Regulatory compliance and customs-related administrative burdens also increased, raising the importance of trade expertise in procurement and contracting. Overall, the tariff environment catalyzed supply chain resilience initiatives, reshaping vendor relationships and accelerating manufacturing localization strategies that will influence procurement negotiation dynamics and product roadmaps in the medium term.

Distinctive segmentation-driven perspectives on modality differentiation, portability trade-offs, clinical application priorities, and end-user procurement behaviors influencing strategic positioning

Interpreting segmentation insights across product type, portability, application, and end-user dimensions provides clarity on where clinical needs and commercial opportunity intersect. Within product categories, computed tomography systems continue to evolve with distinctions between high-slice, mid-slice, and low-slice systems shaping use cases from advanced cross-sectional vascular studies to routine emergency diagnostics. Magnetic resonance imaging equipment remains divided between closed systems optimized for higher field strengths and open systems that prioritize patient comfort and interventional access. Nuclear imaging splits across PET and SPECT modalities, with PET maintaining strength in molecular oncology and SPECT serving broader cardiology and functional imaging indications. Ultrasound retains broad clinical utility with 2D imaging for general diagnostics, 3D and 4D platforms advancing obstetrical and fetal visualization, and Doppler systems enhancing vascular and cardiac flow assessment. X-ray systems continue their transition from analog platforms to digital radiography, improving image workflow and integration with PACS and reporting systems.

Portability defines a separate axis of differentiation, where fixed imaging equipment supports high-throughput centralized services while portable imaging equipment, spanning handheld devices and transportable units, enables decentralized diagnostics and rapid response in emergency or remote settings. Application-driven segmentation reveals modality adoption aligned to clinical domains: cardiology leverages coronary and vascular imaging for interventional planning and follow-up, neurology applies brain and spinal cord imaging for stroke and degenerative disease management, obstetrics and gynecology emphasize fetal monitoring and pelvic imaging, oncology requires early detection and staging plus ongoing monitoring, and orthopedics depends on fracture detection and joint-focused examinations. End-user segmentation likewise informs procurement cadence and service expectations; ambulatory care centers prioritize cost-effective, rapid turnaround systems, diagnostic imaging centers focus on specialized throughput and modality mix, and hospitals and clinics demand versatile, integrated platforms capable of supporting a wide range of acute and elective procedures. Understanding these segment intersections is critical for product positioning, capital planning, and clinical engagement strategies, as modality choice and configuration directly influence clinical workflow, staffing, and downstream revenue generation.

How regional healthcare infrastructure, regulatory fragmentation, and investment priorities are directing differential adoption and commercial strategies across global markets

Regional dynamics exert significant influence on adoption curves, regulatory approaches, and innovation diffusion across the diagnostic imaging industry. In the Americas, established healthcare infrastructure, consolidated vendor footprints, and advanced reimbursement frameworks support rapid uptake of high-end modalities and integrated software solutions, while systems procurement is often tied to demonstrated clinical outcomes and vendor service quality. In Europe, the Middle East & Africa, regulatory fragmentation and heterogeneous reimbursement environments create a patchwork of adoption, where advanced therapies and high-end devices perform strongly in developed pockets while other markets emphasize cost-effective, robust solutions. Policy shifts and centralized purchasing in some jurisdictions further influence pricing and tendering behaviors. In the Asia-Pacific region, investment in healthcare infrastructure, rising clinical demand, and favorable public health initiatives are driving accelerated adoption of both high-end modalities and portable imaging solutions, with several markets showing particular appetite for localized manufacturing partnerships and value-aligned service offerings.

Cross-region supply chain considerations, clinical training availability, and variations in patient demographics all shape how device lifecycles, service models, and aftermarket support are structured. Vendors and providers operating across regions must therefore calibrate product portfolios, financing options, and clinical education programs to local reimbursement realities and infrastructure constraints. Strategic regional partnerships and adaptable go-to-market models are essential to translate global innovation into sustainable regional adoption and to mitigate risks associated with regulatory changes and trade disruptions.

An incisive view of how incumbent manufacturers, nimble innovators, and software disruptors are shaping competitive dynamics through partnerships, services, and modular product strategies

The competitive landscape in diagnostic imaging is characterized by a mix of established multinational manufacturers, specialized niche innovators, and a growing cohort of software-first entrants focused on analytics and workflow optimization. Incumbent device manufacturers continue to emphasize integrated hardware-software bundles, lifecycle service agreements, and financing solutions that reduce adoption friction for large providers. Simultaneously, smaller firms and startups are carving out differentiation through focused clinical applications, disruptive form factors such as handheld ultrasound, and advanced image processing algorithms that can be deployed as cloud-enabled services.

Strategic partnerships, co-development agreements, and targeted acquisitions have emerged as primary levers for both scale and innovation. Many companies are investing in modular architectures that allow incremental feature upgrades, thereby extending product lifespans and creating recurring revenue through software subscriptions and clinical decision support tools. Aftermarket services and managed equipment programs are gaining prominence as revenue-stable offerings that align vendor incentives with provider uptime and performance. As competition intensifies, market leaders are balancing capital-intensive R&D with go-to-market investments in clinical validation, training programs, and customer success teams to accelerate adoption and capture downstream service revenue.

Practical and prioritized strategic actions that vendors and providers should implement to innovate, de-risk supply chains, and align commercial models with clinical outcomes

Industry leaders should adopt a multi-faceted strategy that balances innovation with supply chain resilience and customer-centric commercial models. Prioritizing investments in software and analytics can create differentiated clinical value while enabling recurring revenue through subscription services. At the same time, diversifying supplier bases and evaluating nearshoring or regional manufacturing partnerships will mitigate exposure to trade disruptions and input-cost volatility. Leaders should also reconsider traditional sales approaches by offering configurable financing, outcome-linked contracts, and comprehensive managed-service packages that align incentives with provider performance goals.

Operationally, building strong clinical validation programs and clinician-focused training will accelerate technology adoption and build long-term loyalty. Vendor teams should invest in interoperability and open-architecture designs to ease integration into heterogeneous hospital ecosystems and to support multi-vendor workflows. Finally, companies must integrate sustainability and dose-optimization features into product roadmaps as procurement committees increasingly weigh environmental and patient-safety credentials. By combining technical innovation with flexible commercial models and resilient operations, industry leaders can capture strategic growth while delivering measurable clinical and financial value to customers.

A robust mixed-methods research approach combining stakeholder interviews, clinical literature analysis, and scenario validation to ensure reliable and actionable insights

The research underpinning these insights blended qualitative and quantitative rigor through a structured methodology designed to triangulate evidence and ensure reproducibility. Primary research included structured interviews with clinicians, procurement officers, biomedical engineers, and industry executives, providing frontline perspectives on modality utilization, maintenance cycles, and purchase decision criteria. Secondary research encompassed peer-reviewed clinical studies, regulatory guidance documents, manufacturer technical specifications, and publicly available financial disclosures, which together informed assessments of technology readiness, clinical utility, and operational constraints.

Data synthesis employed cross-validation techniques to reconcile divergent views and to identify consensus trends. Case studies and real-world implementations were analyzed to extract lessons on deployment barriers and success factors. The methodology also incorporated scenario analysis to stress-test strategic assumptions under differing regulatory and supply chain conditions. Limitations were acknowledged, including variations in local reimbursement practices and the dynamic nature of software-driven innovation, and these were addressed through continuous stakeholder engagement and iterative validation cycles to maintain relevance and accuracy.

A concise synthesis of the converging technological, operational, and policy forces that will determine competitive success and clinical impact in diagnostic imaging

In synthesis, the diagnostic imaging equipment sector is at an inflection point where technological advances, shifting care delivery models, and supply chain realities are jointly redefining value creation. Innovations in software, image analytics, and portable hardware are unlocking new clinical use cases and enabling decentralized care workflows, while procurement strategies are increasingly guided by total cost of ownership, clinical outcome linkage, and service continuity. Trade policy and tariff changes have underscored the importance of supply chain diversification and have accelerated regional manufacturing conversations, adding a strategic layer to procurement and product design decisions.

Organizations that successfully integrate product innovation with resilient operations, flexible commercial frameworks, and clinician-centered implementation plans will gain competitive advantage. Moreover, the ability to validate clinical impact, ensure regulatory compliance across jurisdictions, and provide reliable aftermarket services will determine long-term vendor-provider relationships. As the sector continues to evolve, stakeholders should maintain agility in portfolio planning and prioritize investments that deliver demonstrable clinical benefit and operational efficiency across diverse care settings.

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 AI-driven image analysis software in diagnostic imaging workflows to improve accuracy and efficiency
• 5.2. Rapid adoption of photon-counting CT scanners for enhanced spatial resolution and reduced radiation dose
• 5.3. Development of portable and handheld ultrasound devices enabling point-of-care diagnostics in remote settings
• 5.4. Increasing deployment of hybrid PET/MRI systems for simultaneous metabolic and structural imaging in oncology
• 5.5. Expansion of cloud-based PACS solutions with secure data sharing and AI-powered diagnostic support tools

6. Cumulative Impact of United States Tariffs 2025

7. Cumulative Impact of Artificial Intelligence 2025

8. Diagnostic Imaging Equipment Market, by Product Type

• 8.1. Computed Tomography (CT) Scanners
  • 8.1.1. High-Slice CT Scanners
  • 8.1.2. Low-Slice CT Scanners
  • 8.1.3. Mid-Slice CT Scanners
• 8.2. Magnetic Resonance Imaging (MRI) Equipment
  • 8.2.1. Closed MRI Systems
  • 8.2.2. Open MRI Systems
• 8.3. Nuclear Imaging Equipment
  • 8.3.1. PET Systems
  • 8.3.2. SPECT Systems
• 8.4. Ultrasound Systems
  • 8.4.1. 2D Ultrasound Systems
  • 8.4.2. 3D & 4D Ultrasound Systems
  • 8.4.3. Doppler Ultrasound Systems
• 8.5. X-Ray Systems
  • 8.5.1. Analog X-Ray Systems
  • 8.5.2. Digital X-Ray Systems

9. Diagnostic Imaging Equipment Market, by Portability

• 9.1. Fixed Imaging Equipment
• 9.2. Portable Imaging Equipment
  • 9.2.1. Handheld Portable Devices
  • 9.2.2. Transportable Equipment

10. Diagnostic Imaging Equipment Market, by Application

• 10.1. Cardiology
  • 10.1.1. Coronary Imaging
  • 10.1.2. Vascular Imaging
• 10.2. Neurology
  • 10.2.1. Brain Scans
  • 10.2.2. Spinal Cord Imaging
• 10.3. Obstetrics & Gynecology
  • 10.3.1. Fetal Monitoring
  • 10.3.2. Pelvic Imaging
• 10.4. Oncology
  • 10.4.1. Early Detection
  • 10.4.2. Staging & Monitoring
• 10.5. Orthopedics
  • 10.5.1. Fracture Detection
  • 10.5.2. Joint Examination

11. Diagnostic Imaging Equipment Market, by End-User

• 11.1. Ambulatory Care Centers
• 11.2. Diagnostic Imaging Centers
• 11.3. Hospitals & Clinics

12. Diagnostic Imaging Equipment 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. Diagnostic Imaging Equipment Market, by Group

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

14. Diagnostic Imaging Equipment 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. Agfa-Gevaert Group
  • 15.3.2. Analogic Corporation
  • 15.3.3. Avonix Imaging, LLC by Nikon Corporation
  • 15.3.4. Barco NV
  • 15.3.5. Bracco S.p.A.
  • 15.3.6. Canon Medical Systems Corporation
  • 15.3.7. Carestream Health, Inc.
  • 15.3.8. Esaote S.p.A
  • 15.3.9. FUJIFILM Holdings Corporation
  • 15.3.10. GE HealthCare Technologies Inc.
  • 15.3.11. Hologic, Inc.
  • 15.3.12. Konica Minolta, Inc.
  • 15.3.13. Koninklijke Philips N.V.
  • 15.3.14. Medtronic PLC
  • 15.3.15. MinFound Medical Systems Co., Ltd.
  • 15.3.16. Neusoft Corporation
  • 15.3.17. Planmed Oy
  • 15.3.18. Samsung Electronics Co., Ltd
  • 15.3.19. Shanghai United Imaging Healthcare Co., Ltd.
  • 15.3.20. Shenzhen Mindray Bio-Medical Electronics Co Ltd
  • 15.3.21. Shenzhen SONTU Medical Imaging Equipment Co., Ltd.
  • 15.3.22. Shimadzu Corporation
  • 15.3.23. Siemens Healthineers
  • 15.3.24. Stryker Corporation
  • 15.3.25. Ziehm Imaging GmbH