Surgical Incision Closures Market by Product Type (Hemostats, Staples, Sutures), Indication (Cardiovascular, General Surgery, Gynecology), Wound Type, End User, Application - Global Forecast 2025-2032
Description
The Surgical Incision Closures Market was valued at USD 16.74 billion in 2024 and is projected to grow to USD 17.94 billion in 2025, with a CAGR of 7.50%, reaching USD 29.85 billion by 2032.
An incisive introduction to surgical incision closures that frames clinical priorities, innovation drivers, and strategic imperatives for healthcare stakeholders
Surgical incision closures remain a foundational element of operative success, influencing patient outcomes, procedural efficiency, and postoperative resource utilization. This introduction establishes the clinical and commercial context for stakeholders who influence procurement, research and development, and policy. It emphasizes the interplay between device innovation, clinician technique adoption, and institutional imperatives that together shape how closures are selected and applied in diverse care settings.
Contemporary practice is defined by a push toward minimizing tissue trauma, reducing procedure time, and improving infection prevention. Concurrently, manufacturers are advancing material science, delivery systems, and adjunct technologies to meet rising expectations for performance, safety, and ease of use. From the vantage point of hospital leadership and surgical teams, closures are evaluated not only on clinical effectiveness but also on total cost of care and alignment with care pathways. Therefore, a strategic understanding of product portfolios, end-user dynamics, and regulatory environments is essential for decision-makers seeking to optimize outcomes and differentiate offerings in a competitive landscape.
How transformative shifts in technology, clinician preference, reimbursement dynamics, and supply chains are redefining surgical incision closure practice and strategy
The landscape of surgical incision closures is being reshaped by several converging forces that together create opportunities and imperatives for both providers and suppliers. Technological advances in biomaterials, powered delivery systems, and combination hemostat-sealant products are enabling clinicians to tailor closure approaches to tissue type, wound contamination risk, and patient comorbidity. At the same time, clinician preference is migrating toward solutions that reduce operating time and cognitive burden, which drives demand for intuitive devices and streamlined protocols.
Reimbursement and procurement dynamics are shifting incentives toward value-based decision-making, encouraging trials of products that demonstrably reduce complications and length of stay. Supply chain resilience is now a strategic priority following recent global disruptions, prompting healthcare organizations to reassess sourcing, vendor diversification, and inventory strategies. Together, these shifts necessitate integrated approaches that align product design with real-world clinical workflows, regulatory pathways, and payer expectations. As a result, companies that can deliver clinically differentiated products supported by robust evidence and scalable distribution models will gain traction in this evolving market.
Evaluating the cumulative impact of United States tariff changes announced for 2025 on supply chains, procurement timelines, and clinical adoption across closure modalities
United States tariff changes slated for 2025 introduce a new layer of complexity to the procurement and supply strategies surrounding surgical incision closure products. Tariff adjustments can influence landed costs for imported raw materials and finished goods, creating ripple effects across pricing negotiations, contract structures, and vendor selection. These changes are likely to prompt hospitals and health systems to re-evaluate supplier portfolios with an emphasis on geographic diversification, nearshoring options, and inventory buffers to preserve continuity of care.
In addition, manufacturers may respond to tariff pressures by optimizing local manufacturing footprints, renegotiating supplier agreements, or accelerating product redesigns to use domestically sourced components where feasible. Procurement teams will need to intensify scenario planning and incorporate tariff sensitivity into total cost of ownership assessments. From a clinical adoption standpoint, sudden cost shifts could alter the perceived value proposition of higher-cost, innovative closure systems relative to traditional methods. Consequently, stakeholders should anticipate a period of adjustment during which contractual agility, transparent cost modeling, and close collaboration between clinical, supply chain, and finance teams will be critical to maintaining both fiscal control and quality of care.
Deconstructing the market through nuanced segmentation across product types, end users, applications, indications, and wound classes to guide targeted strategy
A robust segmentation framework is essential for understanding where clinical need and commercial opportunity align within the surgical incision closures domain. Based on Product Type, the market is studied across Hemostats, Staples, Sutures, and Tissue Adhesives; Hemostats are further examined across Absorbable Gelatin Sponges, Oxidized Regenerated Cellulose, and Thrombin Based; Staples are differentiated into Manual and Powered variants; Sutures are divided into Absorbable and Non Absorbable categories, with Absorbable further segmented into Poliglecaprone, Polydioxanone, and Polyglycolic Acid, and Non Absorbable split into Nylon, Polypropylene, and Silk; Tissue Adhesives are analyzed across Cyanoacrylate Adhesives, Fibrin Sealants, and Polyethylene Glycol Sealants. This product-level granularity supports targeted product development and clinical training initiatives.
Based on End User, the market is examined across Ambulatory Surgical Centers, Clinics, Home Care, and Hospitals; Clinics are further studied across Multi Specialty and Single Specialty practices, while Hospitals are disaggregated into Private and Public institutions. This end-user differentiation highlights the operational constraints and purchasing behavior unique to each care setting, informing distribution and service models. Based on Application, the market is studied across External and Internal use cases, which directly affects device design, regulatory requirements, and clinician training needs. Based on Indication, the market encompasses Cardiovascular, General Surgery, Gynecology, Neurosurgery, Orthopedic, and Pediatric procedures, reflecting varied tissue types and hemostatic demands. Finally, based on Wound Type, the market is classified across Clean, Clean Contaminated, Contaminated, and Dirty wounds, each of which imposes different infection-control and material-selection considerations. Together, these segmentation layers enable strategic prioritization of R&D, evidence generation, and commercialization efforts to match clinical realities.
Regional dynamics and growth vectors across the Americas, Europe Middle East & Africa and Asia-Pacific that shape procurement, clinical adoption, and training priorities
Regional dynamics exert a profound influence on product adoption patterns, regulatory complexity, and commercial strategies. In the Americas, procurement sophistication and large integrated health systems drive demand for comprehensive value propositions that couple clinical performance data with supply chain reliability and service offerings. The emphasis in this region is often on standardization across networks, formulary alignment, and measurable improvements in patient throughput and complication rates.
In Europe, Middle East & Africa, heterogeneity across national regulatory regimes, reimbursement models, and hospital structures requires flexible market-entry approaches. Localization of clinical evidence, training partnerships, and thoughtfully structured distribution agreements are critical for uptake. In parallel, the region presents opportunities for products positioned to address workforce constraints and to improve outcomes in diverse care settings. Asia-Pacific demonstrates rapid clinical modernization in several markets alongside varying levels of healthcare infrastructure. Here, scalable manufacturing strategies, competitive pricing models, and collaborations that adapt products to local procedural norms can facilitate wider adoption. Across regions, cross-border supply considerations and evolving regulatory expectations mean that manufacturers must balance standardized global platforms with localized execution plans.
Competitive landscape insights focusing on multinational manufacturers, specialty device firms, and innovative startups driving product differentiation and go-to-market approaches
Competitive dynamics in the surgical incision closures field are characterized by a mix of established multinational medical device manufacturers, specialized surgical device firms, and agile startups bringing novel materials or delivery systems to market. Established players benefit from broad distribution networks, long-standing hospital relationships, and extensive clinical evidence portfolios, which can ease pathway-to-adoption in large health systems. Specialized firms often compete through focused innovation, rapid iteration cycles, and deep engagement with clinician opinion leaders, enabling them to capture niche segments where performance differentiation is most valued.
Startups contribute to the landscape by pushing material science boundaries and introducing disruptive delivery mechanisms that can alter practice patterns. Across the competitive set, differentiation increasingly hinges on integrated value propositions that combine device performance with training programs, real-world evidence collection, and service-level commitments. Partnerships, licensing agreements, and targeted acquisitions remain common strategies for accelerating time-to-market and expanding product portfolios. For decision-makers, understanding each competitor’s route-to-market, evidence generation strategy, and partnership ecosystem is essential for anticipating shifts in positioning and for identifying potential alliance or consolidation opportunities.
Actionable recommendations for industry leaders to align R&D, procurement, and commercialization strategies with evolving clinical needs and regulatory expectations
Industry leaders should focus on cohesive strategies that align product innovation with clinical workflows, procurement realities, and regulatory trajectories. First, prioritize the development of clinical evidence that demonstrates not only efficacy but also downstream impacts such as reduced complications and resource use, thereby strengthening value-based conversations with payers and health systems. Second, invest in modular product platforms and device ergonomics that simplify training and minimize intraoperative variability, which will increase uptake among busy surgical teams. Third, build resilient supply chain architectures that include nearshoring options, multiple sourcing strategies, and transparent cost models to mitigate tariff and disruption risks.
Moreover, cultivate strategic partnerships with early adopter clinical institutions to generate real-world data and refine value narratives. Deploy segmented commercial models that differentiate offerings between hospitals, ambulatory surgical centers, clinics, and home-care environments to better match service expectations and procurement practices. Finally, embed regulatory intelligence and reimbursement expertise early in the product lifecycle to accelerate approvals and to reduce time-to-adoption. Taken together, these actions will position organizations to capture clinical credibility while maintaining commercial agility in a rapidly evolving environment.
Transparent research methodology detailing data sources, expert consultations, and analytical frameworks used to ensure rigorous and reproducible insights for decision-makers
This research draws on a multi-method approach that integrates primary expert consultations, secondary literature synthesis, and structured analytical frameworks to ensure validity and transparency. Primary inputs include interviews with surgeons, procurement leaders, and clinical educators across care settings to capture first-hand experience with closure materials and devices. Secondary sources encompass peer-reviewed clinical literature, regulatory filings, and publicly available guidance that inform product risk profiles and comparative performance attributes. These inputs are triangulated to identify consistent themes, divergence points, and areas where evidence gaps persist.
Analytical frameworks applied include segmentation analysis, scenario planning to assess tariff and supply chain impacts, and competitive mapping to elucidate positioning and capability differentials. Data quality is assured through source cross-validation and methodological transparency, and findings emphasize reproducibility by documenting assumptions and analytical steps. Where expert opinion informs interpretation, the methodology distinguishes anecdotal insight from consensus-based observations. This combined approach provides a defensible foundation for strategic decision-making while highlighting priorities for further primary data collection or targeted clinical evaluation.
Conclusive observations synthesizing clinical, commercial, and geopolitical factors to help executives prioritize investments, partnerships, and operating model adaptations
In conclusion, the surgical incision closures landscape is at an inflection point where material innovation, clinician workflow optimization, and external pressures such as tariff changes converge to reshape adoption and procurement dynamics. Success for manufacturers and health systems alike will depend on aligning product design with the realities of varied care settings, producing high-quality clinical evidence that speaks to both efficacy and system-level value, and maintaining flexible supply chains that can absorb geopolitical and policy shocks. Strategic clarity around segmentation and regional execution will enable better allocation of R&D and commercial resources.
Executives should therefore prioritize evidence-driven commercialization, robust clinician engagement, and contingency planning that addresses potential cost disruptions. By doing so, organizations can enhance patient outcomes while achieving sustainable commercial performance in a market that rewards demonstrable clinical benefits and operational reliability.
Note: PDF & Excel + Online Access - 1 Year
An incisive introduction to surgical incision closures that frames clinical priorities, innovation drivers, and strategic imperatives for healthcare stakeholders
Surgical incision closures remain a foundational element of operative success, influencing patient outcomes, procedural efficiency, and postoperative resource utilization. This introduction establishes the clinical and commercial context for stakeholders who influence procurement, research and development, and policy. It emphasizes the interplay between device innovation, clinician technique adoption, and institutional imperatives that together shape how closures are selected and applied in diverse care settings.
Contemporary practice is defined by a push toward minimizing tissue trauma, reducing procedure time, and improving infection prevention. Concurrently, manufacturers are advancing material science, delivery systems, and adjunct technologies to meet rising expectations for performance, safety, and ease of use. From the vantage point of hospital leadership and surgical teams, closures are evaluated not only on clinical effectiveness but also on total cost of care and alignment with care pathways. Therefore, a strategic understanding of product portfolios, end-user dynamics, and regulatory environments is essential for decision-makers seeking to optimize outcomes and differentiate offerings in a competitive landscape.
How transformative shifts in technology, clinician preference, reimbursement dynamics, and supply chains are redefining surgical incision closure practice and strategy
The landscape of surgical incision closures is being reshaped by several converging forces that together create opportunities and imperatives for both providers and suppliers. Technological advances in biomaterials, powered delivery systems, and combination hemostat-sealant products are enabling clinicians to tailor closure approaches to tissue type, wound contamination risk, and patient comorbidity. At the same time, clinician preference is migrating toward solutions that reduce operating time and cognitive burden, which drives demand for intuitive devices and streamlined protocols.
Reimbursement and procurement dynamics are shifting incentives toward value-based decision-making, encouraging trials of products that demonstrably reduce complications and length of stay. Supply chain resilience is now a strategic priority following recent global disruptions, prompting healthcare organizations to reassess sourcing, vendor diversification, and inventory strategies. Together, these shifts necessitate integrated approaches that align product design with real-world clinical workflows, regulatory pathways, and payer expectations. As a result, companies that can deliver clinically differentiated products supported by robust evidence and scalable distribution models will gain traction in this evolving market.
Evaluating the cumulative impact of United States tariff changes announced for 2025 on supply chains, procurement timelines, and clinical adoption across closure modalities
United States tariff changes slated for 2025 introduce a new layer of complexity to the procurement and supply strategies surrounding surgical incision closure products. Tariff adjustments can influence landed costs for imported raw materials and finished goods, creating ripple effects across pricing negotiations, contract structures, and vendor selection. These changes are likely to prompt hospitals and health systems to re-evaluate supplier portfolios with an emphasis on geographic diversification, nearshoring options, and inventory buffers to preserve continuity of care.
In addition, manufacturers may respond to tariff pressures by optimizing local manufacturing footprints, renegotiating supplier agreements, or accelerating product redesigns to use domestically sourced components where feasible. Procurement teams will need to intensify scenario planning and incorporate tariff sensitivity into total cost of ownership assessments. From a clinical adoption standpoint, sudden cost shifts could alter the perceived value proposition of higher-cost, innovative closure systems relative to traditional methods. Consequently, stakeholders should anticipate a period of adjustment during which contractual agility, transparent cost modeling, and close collaboration between clinical, supply chain, and finance teams will be critical to maintaining both fiscal control and quality of care.
Deconstructing the market through nuanced segmentation across product types, end users, applications, indications, and wound classes to guide targeted strategy
A robust segmentation framework is essential for understanding where clinical need and commercial opportunity align within the surgical incision closures domain. Based on Product Type, the market is studied across Hemostats, Staples, Sutures, and Tissue Adhesives; Hemostats are further examined across Absorbable Gelatin Sponges, Oxidized Regenerated Cellulose, and Thrombin Based; Staples are differentiated into Manual and Powered variants; Sutures are divided into Absorbable and Non Absorbable categories, with Absorbable further segmented into Poliglecaprone, Polydioxanone, and Polyglycolic Acid, and Non Absorbable split into Nylon, Polypropylene, and Silk; Tissue Adhesives are analyzed across Cyanoacrylate Adhesives, Fibrin Sealants, and Polyethylene Glycol Sealants. This product-level granularity supports targeted product development and clinical training initiatives.
Based on End User, the market is examined across Ambulatory Surgical Centers, Clinics, Home Care, and Hospitals; Clinics are further studied across Multi Specialty and Single Specialty practices, while Hospitals are disaggregated into Private and Public institutions. This end-user differentiation highlights the operational constraints and purchasing behavior unique to each care setting, informing distribution and service models. Based on Application, the market is studied across External and Internal use cases, which directly affects device design, regulatory requirements, and clinician training needs. Based on Indication, the market encompasses Cardiovascular, General Surgery, Gynecology, Neurosurgery, Orthopedic, and Pediatric procedures, reflecting varied tissue types and hemostatic demands. Finally, based on Wound Type, the market is classified across Clean, Clean Contaminated, Contaminated, and Dirty wounds, each of which imposes different infection-control and material-selection considerations. Together, these segmentation layers enable strategic prioritization of R&D, evidence generation, and commercialization efforts to match clinical realities.
Regional dynamics and growth vectors across the Americas, Europe Middle East & Africa and Asia-Pacific that shape procurement, clinical adoption, and training priorities
Regional dynamics exert a profound influence on product adoption patterns, regulatory complexity, and commercial strategies. In the Americas, procurement sophistication and large integrated health systems drive demand for comprehensive value propositions that couple clinical performance data with supply chain reliability and service offerings. The emphasis in this region is often on standardization across networks, formulary alignment, and measurable improvements in patient throughput and complication rates.
In Europe, Middle East & Africa, heterogeneity across national regulatory regimes, reimbursement models, and hospital structures requires flexible market-entry approaches. Localization of clinical evidence, training partnerships, and thoughtfully structured distribution agreements are critical for uptake. In parallel, the region presents opportunities for products positioned to address workforce constraints and to improve outcomes in diverse care settings. Asia-Pacific demonstrates rapid clinical modernization in several markets alongside varying levels of healthcare infrastructure. Here, scalable manufacturing strategies, competitive pricing models, and collaborations that adapt products to local procedural norms can facilitate wider adoption. Across regions, cross-border supply considerations and evolving regulatory expectations mean that manufacturers must balance standardized global platforms with localized execution plans.
Competitive landscape insights focusing on multinational manufacturers, specialty device firms, and innovative startups driving product differentiation and go-to-market approaches
Competitive dynamics in the surgical incision closures field are characterized by a mix of established multinational medical device manufacturers, specialized surgical device firms, and agile startups bringing novel materials or delivery systems to market. Established players benefit from broad distribution networks, long-standing hospital relationships, and extensive clinical evidence portfolios, which can ease pathway-to-adoption in large health systems. Specialized firms often compete through focused innovation, rapid iteration cycles, and deep engagement with clinician opinion leaders, enabling them to capture niche segments where performance differentiation is most valued.
Startups contribute to the landscape by pushing material science boundaries and introducing disruptive delivery mechanisms that can alter practice patterns. Across the competitive set, differentiation increasingly hinges on integrated value propositions that combine device performance with training programs, real-world evidence collection, and service-level commitments. Partnerships, licensing agreements, and targeted acquisitions remain common strategies for accelerating time-to-market and expanding product portfolios. For decision-makers, understanding each competitor’s route-to-market, evidence generation strategy, and partnership ecosystem is essential for anticipating shifts in positioning and for identifying potential alliance or consolidation opportunities.
Actionable recommendations for industry leaders to align R&D, procurement, and commercialization strategies with evolving clinical needs and regulatory expectations
Industry leaders should focus on cohesive strategies that align product innovation with clinical workflows, procurement realities, and regulatory trajectories. First, prioritize the development of clinical evidence that demonstrates not only efficacy but also downstream impacts such as reduced complications and resource use, thereby strengthening value-based conversations with payers and health systems. Second, invest in modular product platforms and device ergonomics that simplify training and minimize intraoperative variability, which will increase uptake among busy surgical teams. Third, build resilient supply chain architectures that include nearshoring options, multiple sourcing strategies, and transparent cost models to mitigate tariff and disruption risks.
Moreover, cultivate strategic partnerships with early adopter clinical institutions to generate real-world data and refine value narratives. Deploy segmented commercial models that differentiate offerings between hospitals, ambulatory surgical centers, clinics, and home-care environments to better match service expectations and procurement practices. Finally, embed regulatory intelligence and reimbursement expertise early in the product lifecycle to accelerate approvals and to reduce time-to-adoption. Taken together, these actions will position organizations to capture clinical credibility while maintaining commercial agility in a rapidly evolving environment.
Transparent research methodology detailing data sources, expert consultations, and analytical frameworks used to ensure rigorous and reproducible insights for decision-makers
This research draws on a multi-method approach that integrates primary expert consultations, secondary literature synthesis, and structured analytical frameworks to ensure validity and transparency. Primary inputs include interviews with surgeons, procurement leaders, and clinical educators across care settings to capture first-hand experience with closure materials and devices. Secondary sources encompass peer-reviewed clinical literature, regulatory filings, and publicly available guidance that inform product risk profiles and comparative performance attributes. These inputs are triangulated to identify consistent themes, divergence points, and areas where evidence gaps persist.
Analytical frameworks applied include segmentation analysis, scenario planning to assess tariff and supply chain impacts, and competitive mapping to elucidate positioning and capability differentials. Data quality is assured through source cross-validation and methodological transparency, and findings emphasize reproducibility by documenting assumptions and analytical steps. Where expert opinion informs interpretation, the methodology distinguishes anecdotal insight from consensus-based observations. This combined approach provides a defensible foundation for strategic decision-making while highlighting priorities for further primary data collection or targeted clinical evaluation.
Conclusive observations synthesizing clinical, commercial, and geopolitical factors to help executives prioritize investments, partnerships, and operating model adaptations
In conclusion, the surgical incision closures landscape is at an inflection point where material innovation, clinician workflow optimization, and external pressures such as tariff changes converge to reshape adoption and procurement dynamics. Success for manufacturers and health systems alike will depend on aligning product design with the realities of varied care settings, producing high-quality clinical evidence that speaks to both efficacy and system-level value, and maintaining flexible supply chains that can absorb geopolitical and policy shocks. Strategic clarity around segmentation and regional execution will enable better allocation of R&D and commercial resources.
Executives should therefore prioritize evidence-driven commercialization, robust clinician engagement, and contingency planning that addresses potential cost disruptions. By doing so, organizations can enhance patient outcomes while achieving sustainable commercial performance in a market that rewards demonstrable clinical benefits and operational reliability.
Note: PDF & Excel + Online Access - 1 Year
Table of Contents
183 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. Rising adoption of antimicrobial suture coatings to reduce postoperative infection rates
- 5.2. Integration of smart wound monitoring devices with suture lines for real-time healing data
- 5.3. Growth in demand for barbed sutures enabling knotless tissue approximation in minimally invasive surgeries
- 5.4. Advancements in biodegradable polymer-based closures for improved patient wound healing outcomes
- 5.5. Expansion of robotic-assisted suture placement techniques increasing precision in complex procedures
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Surgical Incision Closures Market, by Product Type
- 8.1. Hemostats
- 8.1.1. Absorbable Gelatin Sponges
- 8.1.2. Oxidized Regenerated Cellulose
- 8.1.3. Thrombin Based
- 8.2. Staples
- 8.2.1. Manual
- 8.2.2. Powered
- 8.3. Sutures
- 8.3.1. Absorbable
- 8.3.1.1. Poliglecaprone
- 8.3.1.2. Polydioxanone
- 8.3.1.3. Polyglycolic Acid
- 8.3.2. Non Absorbable
- 8.3.2.1. Nylon
- 8.3.2.2. Polypropylene
- 8.3.2.3. Silk
- 8.4. Tissue Adhesives
- 8.4.1. Cyanoacrylate Adhesives
- 8.4.2. Fibrin Sealants
- 8.4.3. Polyethylene Glycol Sealants
- 9. Surgical Incision Closures Market, by Indication
- 9.1. Cardiovascular
- 9.2. General Surgery
- 9.3. Gynecology
- 9.4. Neurosurgery
- 9.5. Orthopedic
- 9.6. Pediatric
- 10. Surgical Incision Closures Market, by Wound Type
- 10.1. Clean
- 10.2. Clean Contaminated
- 10.3. Contaminated
- 10.4. Dirty
- 11. Surgical Incision Closures Market, by End User
- 11.1. Ambulatory Surgical Centers
- 11.2. Clinics
- 11.2.1. Multi Specialty
- 11.2.2. Single Specialty
- 11.3. Home Care
- 11.4. Hospitals
- 11.4.1. Private
- 11.4.2. Public
- 12. Surgical Incision Closures Market, by Application
- 12.1. External
- 12.2. Internal
- 13. Surgical Incision Closures Market, by Region
- 13.1. Americas
- 13.1.1. North America
- 13.1.2. Latin America
- 13.2. Europe, Middle East & Africa
- 13.2.1. Europe
- 13.2.2. Middle East
- 13.2.3. Africa
- 13.3. Asia-Pacific
- 14. Surgical Incision Closures Market, by Group
- 14.1. ASEAN
- 14.2. GCC
- 14.3. European Union
- 14.4. BRICS
- 14.5. G7
- 14.6. NATO
- 15. Surgical Incision Closures Market, by Country
- 15.1. United States
- 15.2. Canada
- 15.3. Mexico
- 15.4. Brazil
- 15.5. United Kingdom
- 15.6. Germany
- 15.7. France
- 15.8. Russia
- 15.9. Italy
- 15.10. Spain
- 15.11. China
- 15.12. India
- 15.13. Japan
- 15.14. Australia
- 15.15. South Korea
- 16. Competitive Landscape
- 16.1. Market Share Analysis, 2024
- 16.2. FPNV Positioning Matrix, 2024
- 16.3. Competitive Analysis
- 16.3.1. 3M Company
- 16.3.2. Arthrex Inc.
- 16.3.3. B. Braun AG
- 16.3.4. Baxter International Inc.
- 16.3.5. Cardinal Health
- 16.3.6. Coloplast A/S
- 16.3.7. ConvaTec Group PLC
- 16.3.8. Corza Medical
- 16.3.9. CP Medical
- 16.3.10. DermaClip US, LLC
- 16.3.11. Dolphin Sutures
- 16.3.12. Grena Ltd.
- 16.3.13. Integra LifeSciences Holdings Corporation
- 16.3.14. Johnson & Johnson Services, Inc.
- 16.3.15. Medline Industries Inc.
- 16.3.16. Medtronic plc
- 16.3.17. Mölnlycke Healthcare
- 16.3.18. Smith & Nephew plc
- 16.3.19. Stryker Corporation
- 16.3.20. Teleflex Incorporated
- 16.3.21. Terumo Corporation
- 16.3.22. Zimmer Biomet Holdings, Inc.
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