North America Endoscopic Hemostasis Market Size, Share and Trends Analysis Report – Industry Overview and Forecast to 2033

North America Endoscopic Hemostasis Market Size

• The North America endoscopic hemostasis Market is expected to reach USD 1563.38 Million by 2033 from USD 880.69 Million in 2025, growing with a CAGR of 7.9% in the forecast period of 2026 to 2033.
• The North America endoscopic hemostasis market is witnessing steady and robust growth, driven by the rising prevalence of gastrointestinal disorders, increasing incidence of colorectal cancer, peptic ulcers, and gastrointestinal bleeding, and the growing adoption of minimally invasive endoscopic procedures across the region..
• Market growth is further supported by stringent clinical guidelines, a strong focus on patient safety and procedural efficacy, and rising demand for advanced hemostatic technologies that improve procedural outcomes and reduce complication rates. Continuous advancements in endoscopic device design, including improved clips, coagulation systems, sprays, and combination therapies, are enhancing precision, ease of use, and clinical effectiveness. Moreover, increasing investments in medical device R&D, technological innovation, and the integration of next-generation materials and energy-based systems are driving product innovation and supporting the long-term growth of the Asia-Pacific endoscopic hemostasis market.

North America Endoscopic hemostasis Market Analysis

• Expanding healthcare infrastructure, rising volumes of endoscopic procedures, and increasing adoption of minimally invasive treatment approaches are fueling strong demand for endoscopic hemostasis devices in North America. Healthcare providers are increasingly incorporating advanced hemostatic technologies to improve procedural efficiency, reduce complication rates, shorten hospital stays, and enhance overall patient outcomes, thereby supporting sustained market growth.
• The U.S. is projected to dominate the North America Endoscopic hemostasis Market, capturing 80.24% market share in 2026, driven by established healthcare infrastructure, high volume of endoscopic procedures, strong adoption of advanced medical technologies, and presence of leading medical device manufacturers. Favorable reimbursement frameworks, a skilled clinical workforce, and continuous investments in healthcare innovation
• U.S. is the fastest-growing country in the North America endoscopic hemostasis market, supported by early adoption of digital health and advanced endoscopy platforms, strong integration of AI-assisted diagnostics and image-guided endoscopic procedures, and a high level of clinical research participation in gastrointestinal and interventional endoscopy. The country’s well-structured referral pathways, emphasis on day-care and outpatient endoscopic treatments, and rapid commercial uptake of next-generation hemostatic devices by clinicians further accelerate procedural volumes. In addition, collaborations between hospitals, academic institutions, and medical device manufacturers, along with streamlined regulatory approval timelines for innovative technologies, continue to position Denmark as a leading early-adopter market, driving faster growth compared to other North America countries.
• The Mechanical hemostasis devices segment is dominating the North America Endoscopic hemostasis Market, accounting for 43.05% market share in 2025. This dominance is driven by the widespread clinical adoption of endoscopic clips and band ligation devices due to their proven efficacy, ease of deployment, cost-effectiveness, and suitability for a broad range of gastrointestinal bleeding indications. Their strong safety profile and compatibility with standard endoscopic procedures continue to support sustained demand across healthcare settings.

Report Scope and North America Endoscopic hemostasis Market Segmentation 

North America Endoscopic Hemostasis Market Trends

“Increasing Adoption of Advanced Minimally Invasive Endoscopic Hemostasis Technologies”

• The steady expansion of endoscopic and minimally invasive procedures across North America is a major factor driving the increased adoption of endoscopic hemostasis devices. As the incidence of gastrointestinal bleeding, colorectal disorders, and related conditions continues to rise, healthcare providers increasingly rely on advanced hemostasis solutions to ensure effective bleeding control, procedural safety, and improved patient outcomes across high-volume clinical environments.
• Endoscopic hemostasis devices play a critical role in ensuring clinical efficacy, patient safety, and procedural reliability throughout diagnostic and therapeutic endoscopy. By enabling rapid bleeding control, reducing complication risks, and supporting minimally invasive treatment approaches, these devices help optimize procedural workflows while improving recovery times and overall quality of care across healthcare facilities.
• The growing adoption of advanced endoscopic technologies, including high-definition imaging, therapeutic endoscopy, and combination hemostasis techniques, has increased demand for high-performance hemostatic solutions. Innovations in mechanical clips, thermal coagulation systems, injection therapies, and topical hemostatic agents are enhancing procedural precision, treatment success rates, and clinician confidence while supporting evolving clinical practices.
• Healthcare providers across the care continuum are increasingly adopting endoscopic hemostasis devices to meet rising regulatory, safety, and clinical performance standards. Stringent clinical guidelines, growing emphasis on patient safety and outcome-based care, and increasing demand for minimally invasive interventions are encouraging hospitals and clinics to integrate advanced hemostasis technologies that ensure consistency, compliance, and high-quality care delivery.
• Overall, the expanding scale of endoscopic procedures, clinical innovation, and healthcare infrastructure development positions endoscopic hemostasis devices as an essential component of modern gastrointestinal care. These solutions support procedural efficiency, patient safety, regulatory compliance, and sustainable growth across North America’s evolving endoscopy landscape, making this insight readily reusable across regions by adapting healthcare system dynamics and adoption patterns.

North America Endoscopic Hemostasis Market Dynamics

Driver

“Rise in Gastrointestinal Bleeding Cases”

• The rising incidence of gastrointestinal bleeding has been established as a foundational force propelling growth in the North America endoscopic hemostasis market. As the prevalence of upper and lower gastrointestinal bleeding conditions increases worldwide, demand for minimally invasive, endoscopy-based therapeutic interventions has been intensified. Endoscopic hemostasis offers critical clinical advantages, including rapid bleeding control, reduced need for surgical intervention, lower transfusion requirements, and shorter hospital stays, thereby positioning it as a first-line treatment modality in acute and chronic gastrointestinal bleeding management. Consequently, the escalation in gastrointestinal bleeding cases—driven by aging populations, higher prevalence of liver disease, anticoagulant use, and delayed care access during systemic healthcare disruptions—has translated into higher procedural volumes and broader adoption of advanced endoscopic hemostasis devices across hospitals and endoscopy centers in North America.

For instances,

• In September 2021, Medscape reported that upper gastrointestinal bleeding occurred at an incidence of approximately 100 cases per 100,000 population annually and remained one of the most common causes of emergency hospital admissions, underscoring a persistently high disease burden requiring endoscopic intervention.
• In June2023, Gastroenterology Research journal reported that mortality related to upper gastrointestinal bleeding in the U.S. increased between 2012 and 2021, with steeper increases observed toward the later years, indicating worsening clinical outcomes and intensified treatment requirements.
• In June 2023, StatPearls Publishing stated that gastrointestinal bleeding continues to represent a frequent North America medical emergency, with urgent endoscopic diagnosis and hemostatic treatment remaining critical to reducing mortality and morbidity.
• In January 2025, the Journal of Clinical Medicine reported that patients with advanced liver disease exhibited significantly higher incidence of massive gastrointestinal bleeding episodes, reinforcing the link between chronic disease prevalence and increased need for endoscopic hemostasis.
• In September 2025, PubMed Central highlighted that upper gastrointestinal bleeding remained a life-threatening complication among chronic liver disease populations, sustaining elevated demand for endoscopic therapeutic procedures.
• The North America escalation in gastrointestinal bleeding incidence is being firmly established as a permanent structural growth engine for the endoscopic hemostasis market. The continuous rise in acute bleeding events, combined with expanding populations affected by chronic liver disease, antithrombotic medication use, and age-related gastrointestinal pathology, is creating a sustained and non-cyclical requirement for endoscopic bleeding control. As clinical guidelines increasingly prioritize endoscopic therapy as first-line management, reliance on hemostasis technologies for emergency intervention, recurrence prevention, and complication management is being structurally reinforced. Furthermore, improving survival rates are extending patient monitoring and repeat intervention cycles, thereby multiplying lifetime procedural demand. This dynamic is anchoring endoscopic hemostasis adoption closely to North America epidemiological trends, positioning this driver as a long-term foundational pillar for market expansion across developed and emerging healthcare systems.

Restraint/Challenge

“High Cost and Technical Complexity of Endoscopic Hemostasis Devices”

• Despite growing clinical adoption, the North America endoscopic hemostasis market continues to face structural restraint due to the high cost and technical complexity of advanced endoscopic hemostasis devices. These technologies often require significant upfront capital investment for equipment procurement, continuous expenditure on consumables, and specialized maintenance. In addition, effective use of hemostatic endoscopic devices demands advanced physician training, skilled support staff, and sophisticated hospital infrastructure, limiting adoption in cost-sensitive healthcare systems. Public hospitals in low- and middle-income countries, and even budget-constrained facilities in developed regions, frequently encounter barriers related to affordability, reimbursement gaps, and workforce readiness. As a result, uneven access and slower penetration of advanced endoscopic hemostasis technologies persist, constraining broader market expansion.

For Instance,

• In November 2022, according to the high cost of gastrointestinal endoscopy procedures and equipment is a major restraint. For example, TNE costs Euro 125.90 per procedure, while oral endoscopy costs Euro 184.10 and MACE costs Euro 407.10. Additionally, equipment maintenance and reprocessing add to the cost, with flexible endoscopes costing around Euro 79,330, making procedures expensive overall.
• In June 2024, Science direct highlighted that the high cost of gastrointestinal endoscopy is exacerbated in low-income and middle-income countries (LICs and LMICs) due to the lack of local maintenance and repair facilities. Scopes requiring repairs must be shipped abroad, incurring significant costs and delays. Additionally, cheaper second-hand and Chinese-manufactured endoscopes often lack adequate service and maintenance support.
• In October 2025, BMJ Open Gastroenterology published a micro-costing study showing that in a UK National Health Service hospital, the total per-procedure cost of reusable gastrointestinal endoscopes was an estimated GBP107.34, with capital and maintenance costs as major cost drivers, highlighting economic barriers to wide adoption of endoscopic equipment in public health settings.
• In August 2024, a ScienceDirect narrative review reported that purchase, maintenance, and associated logistics costs of endoscopy equipment remain a major barrier to developing and sustaining endoscopy services in low- and middle-income countries, due to high device cost and lack of infrastructure.
• In February 2025, as per science direct the high cost of gastrointestinal endoscopy is evident in various studies, especially for screening and surveillance. For instance, while general population screenings may not be cost-effective in Western regions, targeted surveillance for high-risk groups, such as those with gastric intestinal metaplAsia, can still be cost-effective, with ICERs ranging from USD 20,739.1 to 98,402.2 per QALY.
• The compiled evidence clearly indicates that the high cost and technical complexity associated with gastrointestinal endoscopy and endoscopic hemostasis devices represent a persistent restraint on market growth. Substantial capital investment for equipment procurement, elevated per-procedure costs, and ongoing expenses related to maintenance, reprocessing, and repair significantly increase the overall cost burden on healthcare systems. These challenges are further intensified in low- and middle-income regions where limited technical infrastructure and lack of local servicing capabilities delay adoption and restrict procedural capacity. Even in developed healthcare systems, cost-effectiveness considerations influence screening strategies and limit widespread implementation. Collectively, these economic and operational constraints slow penetration of advanced endoscopic hemostasis technologies, reinforcing affordability and technical complexity as structural barriers to broader market expansion

North America Endoscopic Hemostasis Market Scope

The North America endoscopic hemostasis market is categorized into five key segments: product type, procedure, application, end user, and distribution channel.

• By product type

On the basis of product type, the North America endoscopic hemostasis market is segmented into mechanical hemostasis devices, thermal devices, topical agents and injectables, and others. In 2026, the mechanical hemostasis devices segment is projected to dominate the North America Endoscopic hemostasis Market with the largest market share of 43.08%, owing to its widespread clinical preference for achieving immediate, controlled, and durable bleeding cessation during endoscopic interventions. Mechanical solutions such as clips and banding devices are routinely favored for their ability to provide precise vessel closure without inducing thermal tissue damage, thereby lowering rebleeding rates and post-procedure complications. Their applicability across a broad spectrum of bleeding scenarios, including peptic ulcers, variceal hemorrhage, and post-polypectomy bleeding, has resulted in consistently high utilization in both emergency and elective endoscopic settings. The strong reliance on mechanical hemostasis as a first-line therapeutic approach underscores its substantial contribution to overall market revenues and reinforces its dominant position within the product type landscape throughout the forecast period.

The topical agents and injectables segment is the fastest-growing segment in the endoscopic hemostasis market, with a CAGR of 8.3%. Growth is driven by the increasing incidence of gastrointestinal bleeding, widespread adoption of minimally invasive endoscopic procedures, and strong clinical demand for rapid-acting, easy-to-administer hemostatic solutions. Continuous advancements in formulation effectiveness, safety, and procedural efficiency are expected to sustain segment growth during the forecast period.

• By procedure

On the basis of procedure, the market is segmented into upper gastrointestinal endoscopy, lower gastrointestinal endoscopy, bronchoscopic hemostasis, and others. In 2026, the upper gastrointestinal endoscopy segment is projected to dominate the North America Endoscopic hemostasis Market with a market share of 42.81%, due to its extensive clinical adoption as the frontline procedural approach for managing acute and recurrent gastrointestinal bleeding. Upper GI endoscopy is widely relied upon for the diagnosis and immediate therapeutic control of bleeding ulcers, variceal hemorrhage, and Dieulafoy lesions, where rapid hemostatic intervention is clinically critical. The high procedural frequency in emergency departments and tertiary-care hospitals, combined with strong guideline support for early endoscopic intervention, is expected to sustain its leading market position. Its continued dominance is reflected in its substantial market share and steady growth trajectory through 2033, indicating persistent demand across both developed and emerging healthcare systems.

The lower gastrointestinal endoscopy segment is the fastest-growing application segment in the endoscopic hemostasis market, registering a CAGR of 8.3%. This growth is supported by rising prevalence of lower gastrointestinal bleeding conditions, increasing volumes of diagnostic and therapeutic colonoscopy procedures, and improved detection of colorectal disorders. Ongoing technological advancements in endoscopic hemostasis devices and growing emphasis on early diagnosis are expected to further drive adoption during the forecast period.

• By application

On the basis of application, the market is segmented into gastrointestinal bleeding, non-gastrointestinal bleeding, trauma management, and others. In 2026, the gastrointestinal bleeding segment is projected to dominate the North America Endoscopic hemostasis Market with a market share of 71.16%, owing to the high North America prevalence of peptic ulcers, esophageal varices, and colorectal malignancies requiring endoscopic bleeding control. Gastrointestinal bleeding remains the most common indication for endoscopic hemostasis procedures, driving consistent utilization of mechanical, thermal, and topical hemostatic solutions across hospital and ambulatory care settings. The critical need for rapid bleeding control to reduce morbidity, hospital length of stay, and mortality is expected to reinforce sustained demand within this application segment. Its large share of total market value highlights the central role of gastrointestinal indications in shaping overall market dynamics during the forecast period.

The trauma management segment is the fastest-growing segment in the endoscopic hemostasis market, with a CAGR of 8.5%. Growth is driven by the increasing occurrence of acute bleeding associated with traumatic injuries and a growing preference for minimally invasive techniques that enable rapid bleeding control. Improved clinical outcomes, reduced surgical intervention rates, and advancements in emergency endoscopic hemostasis technologies are expected to support continued expansion of this segment over the forecast period.

• By end user

On the basis of end user, the market is segmented into hospitals, ambulatory surgery centers, specialty clinics, and others. In 2026, the hospitals segment is projected to dominate the North America Endoscopic hemostasis Market with the largest market share of 52.06%, due to the concentration of advanced endoscopy infrastructure, skilled gastroenterologists, and emergency care capabilities within hospital settings. Complex bleeding cases, including severe upper and lower gastrointestinal hemorrhage, are predominantly managed in public and private hospitals where comprehensive diagnostic and interventional resources are available. Higher patient inflow, greater procedural volumes, and established procurement frameworks further strengthen hospital demand for endoscopic hemostasis devices and consumables. This structural dependence on hospital-based care is expected to maintain the segment’s leading position through 2033 despite gradual growth in outpatient settings.

The ambulatory surgery centers segment is the fastest-growing end-user segment in the endoscopic hemostasis market, recording a CAGR of 8.3%. Growth is driven by the increasing shift toward outpatient endoscopic procedures, demand for cost-effective healthcare delivery, and shorter patient recovery times. Advancements in compact, efficient hemostasis devices suitable for outpatient settings are expected to further accelerate adoption during the forecast period.

• By distribution channel

On the basis of distribution channel, the market is segmented into direct sales and indirect sales, with indirect sales further segmented into online and offline channels. In 2026, the indirect sales segment is projected to dominate the North America Endoscopic hemostasis Market with the largest market share of 57.93% as procurement is largely conducted through distributors, group purchasing organizations, and regional medical supply networks. Indirect channels are widely preferred due to their ability to offer bundled products, inventory management support, and broader geographic reach, particularly in emerging markets and decentralized healthcare systems. Hospitals and ambulatory centers frequently rely on distributor-led sourcing to ensure consistent availability of critical hemostasis devices while optimizing procurement costs. This distribution structure is expected to continue driving higher adoption of indirect sales channels throughout the forecast period.

The indirect sales segment is the fastest-growing distribution channel in the endoscopic hemostasis market, with a CAGR of 8.1%. This growth is supported by the expanding role of distribution partners and group purchasing networks in enhancing product accessibility and supply efficiency. Increasing reliance on centralized procurement models, bundled purchasing agreements, and regional distributor expertise is expected to continue driving growth of the indirect sales channel throughout the forecast period.

Endoscopic Hemostasis Market Regional Analysis

• U.S. represents one of the most important markets for endoscopic hemostasis devices, supported by its advanced healthcare infrastructure, strong medical device manufacturing base, and high adoption of minimally invasive endoscopic procedures. Continuous clinical innovation in gastroenterology, a high volume of diagnostic and therapeutic endoscopies, and strict clinical and regulatory standards are driving steady adoption of advanced mechanical, thermal, and topical hemostasis solutions across hospitals and specialty care centers.
• Mexico is witnessing growing demand for endoscopic hemostasis technologies as increasing prevalence of gastrointestinal disorders, an aging population, and rising emphasis on minimally invasive treatment approaches reshape clinical practice. Healthcare providers are increasingly focused on improving patient safety, reducing procedure-related complications, and enhancing clinical efficiency, which is accelerating the adoption of reliable and cost-effective hemostasis devices across public and private healthcare settings.
• Canada  continues to emerge as a key growth hub for the endoscopic hemostasis market, driven by strong clinical expertise in gastroenterology, expanding access to advanced endoscopic services, and increasing focus on patient-centered and outcome-driven care. The country’s emphasis on clinical quality, safety, and technological innovation is encouraging healthcare institutions to adopt advanced hemostasis solutions that improve procedural outcomes, support minimally invasive interventions, and comply with evolving regulatory and healthcare standards.

U.S. Endoscopic Hemostasis Market Insight

The U.S. Endoscopic hemostasis Market is gaining strong traction due to the country’s high volume of gastrointestinal endoscopic procedures and early adoption of advanced therapeutic endoscopy techniques. U.S. hospitals and specialty clinics place strong emphasis on clinical precision, procedural reliability, and evidence-based device selection, driving consistent demand for high-performance mechanical and energy-based hemostasis solutions. In addition, the presence of leading medical device manufacturers, well-established clinical training programs, and strict regulatory and quality standards is fostering rapid uptake of technologically advanced hemostasis devices. U.S. focus on procedural standardization, patient safety, and outcome optimization reinforces its position as a technology-led and innovation-driven market within North America.

Canada Endoscopic Hemostasis Market Insight

The Canada Endoscopic hemostasis Market continues to expand as healthcare providers prioritize minimally invasive treatment pathways, efficiency in endoscopy units, and reduction of procedure-related complications. Rising incidence of gastrointestinal bleeding conditions, combined with increasing demand on NHS endoscopy services, is accelerating adoption of cost-effective, easy-to-use hemostasis devices that support high procedural throughput. Strong emphasis on clinical guidelines, value-based care, and standardized treatment protocols is shaping purchasing decisions, while growing use of ambulatory and day-care endoscopy settings is further supporting demand. These factors collectively position the Japan market as one driven by access, efficiency, and scalable clinical adoption rather than device manufacturing concentration.

North America Endoscopic Hemostasis Market Share

The endoscopic hemostasis industry is primarily led by well-established companies, including:

• Micro-Tech Endoscopy (China)
• Taewoong Medical Co., Ltd. (South Korea)
• Ovesco Endoscopy AG (China)
• Apollo Endosurgery, Inc. (U.S.)
• Argon Medical Devices, Inc. (U.S.)
• Olympus Corporation (Japan)
• Boston Scientific Corporation (U.S.)
• CONMED Corporation (U.S.)
• Medtronic (Ireland)
• Cook (U.S.)
• ERBE Elektromedizin GmbH (China)
• Karl Storz SE & Co. KG (China)
• Pentax Medical (Japan)
• Endoskopie Technik Gerhard (China)
• Merit Medical Systems, Inc. (U.S.)
• Diversatek, Inc. (U.S.)
• STERIS plc (JAPAN)
• B. Braun SE (China)
• Duomed Group (Belgium)

Latest Developments in the North America Endoscopic Hemostasis Market

• In December 2025, Olympus tripled its corporate venture capital fund commitment by launching Olympus Innovation Ventures Fund II with an additional $150 million to invest in MedTech startups focused on endoscopy, diagnostics, digital health, and related innovation fields to reinforce long-term growth and technological leadership.
• In October 2025, Boston Scientific announced an agreement to acquire Nalu Medical, Inc., a privately held medical device company focused on implantable neurostimulation technologies for chronic pain. The acquisition was positioned to strengthen Boston Scientific’s neuromodulation portfolio, accelerate innovation in pain management, and expand treatment options for patients with chronic pain conditions.
• In October 2025, CONMED Corporation announced a strategic exit from its gastroenterology business, divesting its GI product lines and related assets as part of a portfolio realignment to concentrate on core surgical and orthopaedic solutions. The move was positioned to streamline the company’s product focus, sharpen investment in high-growth procedural areas, and improve long-term revenue and margin profiles by reallocating resources toward CONMED’s flagship device platforms and emerging technologies.
• In August 2025, the U.S. Food and Drug Administration (FDA) approved the first-of-its-kind IDE clinical study of Cook Medical’s ADVANCE EVERO 18 everolimus-coated PTA balloon catheter, enabling evaluation of its safety and effectiveness in treating symptomatic peripheral arterial disease. The decision marked a milestone for drug-coated balloon technology, supporting Cook’s advancement of next-generation endovascular therapies aimed at reducing restenosis and improving long-term vessel patency in patients with lower-extremity arterial disease.

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