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Hemostasis and Tissue Sealing Agents Market size will register significant growth between 2024 and 2032, fueled by technological advancements from industry leaders. Leading players are driving innovation with the development of advanced solutions for hemostasis and tissue sealing.
In May 2023, KITSS Therapeutics, a Ghanaian medical device and service company, introduced a groundbreaking product named BLOODSTOP and BLOODSTOPiX. This innovative hemostatic solution accelerated clotting time, promptly stopped bleeding, and expedited wound healing. Registered with the Ghanaian Foods and Drugs Administration (FDA), BloodSTOPiX Advanced Hemostat with WoundHEAL is a clinically proven dressing and wound healing matrix. This product aimed to revolutionize wound, surgery, and burn treatment in the Ghanaian medical sector by providing effective and swift hemorrhage control, thereby reducing blood loss.
These technological breakthroughs enhance the effectiveness of medical procedures, reduce complications, and contribute to improved patient outcomes. As a result, the market experiences a surge in demand as healthcare providers seek cutting-edge products to address hemostasis and tissue sealing needs, reflecting the industry's commitment to advancing medical capabilities.
Hemostasis and Tissue Sealing Agents market experiences growing demand due to a surge in product launches from leading companies in the sealant segments. Industry leaders are introducing innovative solutions that enhance hemostasis and tissue sealing. These product launches signify a commitment to addressing evolving healthcare needs, offering advanced options for surgical and medical interventions. As companies in the sealant segments continue to unveil cutting-edge products, the market witnesses increased adoption driven by the pursuit of superior hemostatic and tissue-sealing capabilities in diverse medical applications.
In June 2021, Ethicon, a Johnson & Johnson Medical Devices Company, introduced the ENSEAL X1 Curved Jaw Tissue Sealer, an advanced bipolar energy device. This innovation provided stronger sealing and enhanced procedural efficiency, in line with improved access to more tissue compared to LigaSure™ Maryland. Indicated for gynecological, bariatric, colorectal, and thoracic procedures, the ENSEAL X1 Curved Jaw was the initial offering in a series of advanced laparoscopic bipolar devices planned for launch.
The Hemostasis and Tissue Sealing Agents market encounters restraints stemming from factors like regulatory challenges, high development costs, and limited reimbursement policies. Stringent regulatory approval processes contribute to extended product timelines, hindering market entry. The substantial investment required for research, development, and clinical trials poses challenges, affecting accessibility for some market participants. Additionally, limited reimbursement policies create financial barriers for end-users. Addressing these restraints necessitates strategic approaches to streamline regulatory processes, manage development costs, and advocate for broader reimbursement coverage in the evolving landscape of hemostasis and tissue-sealing agents.
The industry is witnessing a trend marked by increasing partnerships and deals among prominent players. Collaborations between key industry stakeholders are driving innovation and expanding product portfolios in hemostasis and tissue-sealing solutions. These strategic alliances leverage the strengths of each participant, fostering advancements in research, development, and commercialization. The trend reflects a shared commitment to meet evolving healthcare demands through synergies and mutual expertise.
To cite an instance, in May 2023, Olympus Europa SE & Co. KG announced that it is set to launch three Endoclot products, including two hemostatic agents and a submucosal injection agent, across the Europe, Middle East, and Africa (EMEA) region. Developed by Endoclot Plus Inc. in Santa Clara, California, this new portfolio expanded the distribution partnership between Endoclot and Olympus from the U.S. to EMEA, initiated in December 2022. Stefanie Kaufung, EMEA Business Unit Manager for Gastrointestinal Endotherapy at Olympus, expressed the company's commitment to enhancing patient outcomes and advancing the standard of care in gastrointestinal procedures.
The industry share from topical hemostats will showcase significant growth through 2032 attributed to the rising adoption of these agents as they offer non-antigenicity, minimal tissue reactivity, and easy absorbability and work well with conventional treatment. The increasing popularity of fibrin sealants and gelatin sponges will boost product uptake in the forecast timeframe. With applications in various medical procedures and surgeries, topical hemostats contribute to minimizing bleeding and enhancing patient outcomes. The market's increasing reliance on these specialized agents underscores their importance in modern medical practices, reflecting a growing demand for advanced solutions in hemostasis and tissue sealing.
The minimally invasive surgeries segment will witness lucrative expansion up to 2032 with the rising need for faster recovery and shorter hospital stays. Key advantages of minimally invasive surgical techniques, such as fewer operative and post-operative complications, less post-operative pain, faster recovery times, and smaller incisions, are contributing to their demand in the market. The infusion of novel hemostasis technologies is another driver for industry development.
North America is poised to record higher consumption of hemostasis and tissue sealing agents between 2023 and 2032 due to the thriving demand for adhesives and sealants. The higher prevalence of diabetes, CVD, and cancer in the region will also add to the regional market expansion. As per statistics from cdc.gov, over 37 million Americans have diabetes, with nearly 90 to 95% suffering from type 2 diabetes.
Major companies operating in the hemostasis and tissue sealing agents industry competitive landscape include:
These firms invest in R&D to innovate new products with enhanced hemostatic and tissue sealing properties, catering to diverse surgical needs. Strategic partnerships with healthcare institutions and surgical device manufacturers facilitate product integration and market expansion. Also, regulatory compliance and obtaining necessary approvals ensure product safety and market access.
Additionally, targeted marketing efforts and educational initiatives raise awareness among surgeons and healthcare professionals about the benefits of their products. Moreover, continuous improvement in manufacturing processes and supply chain management ensures reliability and cost efficiency. Besides, monitoring market trends and competitive analysis enables companies to adapt swiftly and capitalize on emerging opportunities.
In November 2023, Ethicon, a division of Johnson & Johnson MedTech, received European approval for Ethizia, its hemostatic sealing patch. Ethizia, featuring innovative synthetic polymer technology, was designed to achieve sustained hemostasis in challenging bleeding situations. It is the first hemostatic matrix equally active on both sides, offering adaptability in open and minimally invasive surgeries. The patch is versatile, allowing stuffing, rolling, pulling apart, trimming, and tailoring. In clinical trials, Ethizia demonstrated rapid efficacy, stopping bleeding in 30 seconds for 80% of patients, six times faster than leading fibrin sealant patches.