The Global Biosurgery Market is expected to cross Global 25.08 Billion market size by 2031, with 6.13% CAGR by 2026-31.

  • Historical Period: 2020-2024
  • Base Year: 2025
  • Forecast Period: 2026-2031
  • Market Size (2025): USD 17.71 Billion
  • Market Size (2020): USD 25.08 Billion
  • CAGR (2026-2031): 6.13
  • Largest Market: Albania
  • Fastest Market: Andorra
  • Format: PDF & Excel
Featured Companies
  • 1 . Johnson & Johnson,
  • 2 . Baxter International Inc.
  • 3 . Medtronic plc
  • 4 . Becton, Dickinson and Company
  • 5 . B. Braun Melsungen AG
  • 6 . Integra LifeSciences
  • More...

Biosurgery Market Analysis

The global biosurgery market is driven by rising surgical procedure volumes across all major regions, an aging global population, and the increasing prevalence of chronic diseases including cardiovascular disorders, cancer, and orthopedic conditions. The market encompasses a broad range of biologically derived and bio-compatible materials including hemostatic agents, surgical sealants and adhesives, bone-graft substitutes, adhesion barriers, soft-tissue attachments, and staple-line reinforcement products that assist in surgical procedures by controlling bleeding, sealing tissues, promoting regeneration, and preventing postoperative complications. Clinical adoption is supported by evidence-based surgical guidelines, sophisticated diagnostic capabilities, and growing use of minimally invasive and robotic-assisted surgical techniques across both developed and emerging healthcare systems. According to the research report, "Global Biosurgery Market Outlook, 2031," published by Actual Market Research, the Global Biosurgery Market is expected to cross Global 25.08 Billion market size by 2031, with 6.13% CAGR by 2026-31.. According to the World Health Organization (WHO), about 234 million major surgeries are performed globally each year, covering a broad range of procedures including orthopedic, cardiovascular, general, gynecological, and neurological surgeries. The global surgical procedure volume continues to grow consistently, driven by an aging population, rising disease burden, and expanding healthcare access across emerging economies. Healthcare expenditure averages approximately 10% of GDP in developed nations, with countries like the United States (over 17% of GDP), Germany (12.4% of GDP), Japan (11.68% of GDP), and France (11.5% of GDP) leading global health spending. In emerging markets, healthcare expenditure is rising rapidly, with China reaching 6.8% of GDP in 2025 and India at 3.61% of GDP, providing the financial foundation for sustained surgical activity and biosurgical product utilization. North America dominates the global biosurgery market, driven by the region's high surgical volumes, advanced healthcare infrastructure, robust reimbursement systems, and presence of key global market players. According to estimates, the United States alone performs approximately 40 million to 50 million major surgical procedures annually, with over a million total joint arthroplasties and more than 400,000 spinal fusion procedures performed each year. Asia-Pacific represents the fastest-growing region, supported by massive surgical volumes across China (97.68 million inpatient surgical procedures in 2024), India (estimated 30 million surgeries annually), and other rapidly developing healthcare markets.

Europe maintains a strong market presence, led by Germany with 16.5 million surgical procedures annually, France with more than 9 million surgical interventions, and the United Kingdom with 8.25 million episodes with a procedure in NHS providers in 2025/26. Across all regions, the biosurgery market continues to benefit from technological innovation, including next-generation hemostatic agents with faster action times, synthetic sealants with enhanced wet-tissue adhesion, and bioactive bone grafts with regenerative capabilities. The increasing adoption of minimally invasive and robotic-assisted surgical techniques is creating new opportunities for biosurgical products specifically designed for these applications. Regulatory modernization across major markets including the FDA's accelerated pathways in the United States, China's NMPA innovative device review process, the European Commission's proposed MDR amendments, and regulatory developments in emerging markets is facilitating faster market access for innovative products. North America is expected to retain market leadership, while Asia-Pacific is projected to maintain the fastest growth rate through 2031, supported by expanding healthcare infrastructure, increasing surgical volumes, and broader access to advanced biosurgical products. .

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Market Dynamic

Market Drivers

• Massive and growing surgical volumes across all regions: The global surgical procedure volume continues to expand consistently, with approximately 234 million major surgeries performed annually worldwide according to the World Health Organization. China leads with 97.68 million inpatient surgical procedures in 2024, while the United States performs approximately 40 million to 50 million major surgical procedures annually. India performs an estimated 30 million surgeries annually, while Germany performs 16.5 million inpatient surgical procedures. The breadth and depth of surgical activity across all regions ensure that biosurgical products particularly hemostatic agents and sealants are utilized in virtually every operating room. The continued expansion of surgical capacity, driven by hospital modernization, ambulatory surgical center (ASC) development, and healthcare workforce growth across both developed and emerging economies, further reinforces this demand driver.

• Global aging population and rising chronic disease burden: The aging global population represents the most significant long-term demand driver for biosurgical products. By 2030, one in six people in the world will be aged 60 years or over, rising from 1 billion in 2020 to 1.4 billion. Japan has the highest proportion of elderly globally at 29.4% (36.19 million people aged 65 and older), while Germany has 23.7% of its population aged 65 and older, and Italy has 24.7%. China has 323.38 million people aged 60 and older (23.0% of the population), and India has over 107.98 million people aged 65 and older. The increasing prevalence of chronic diseases, including cardiovascular disorders (which account for approximately 17.9 million deaths annually, or 32% of all global deaths), cancer (projected to reach 35 million new cases by 2050), and orthopedic conditions, is leading to more surgical interventions and driving demand for biosurgical products across all product categories.

• Technological innovation and regulatory modernization: Continuous innovation in biomaterials and surgical delivery systems is expanding the addressable market globally. Next-generation hemostatic agents with faster action times, synthetic sealants with enhanced wet-tissue adhesion, and bioactive bone grafts with regenerative capabilities are creating new clinical applications and premium-pricing opportunities. Regulatory modernization across major markets is facilitating faster market access: the FDA's accelerated pathways in the United States, China's NMPA innovative device review process (which approved 104 devices in 2025), Japan's PMD Act amendments, South Korea's Digital Medical Products Act, and the European Commission's proposed MDR amendments. These developments support continued innovation and market entry for advanced biosurgical products across all regions. Market Challenges

• Pricing pressure and cost-containment initiatives globally: Despite the market's size and growth potential, biosurgery manufacturers face persistent pricing pressure from hospital procurement organizations, group purchasing organizations (GPOs), and government payers across all regions. In China, volume-based procurement (VBP) policies have led to dramatic price reductions in many cases exceeding 80% for selected products, compressing profit margins. In the United States, CMS reimbursement policies exert significant pricing pressure. In Europe, public healthcare systems negotiate centralized pricing. In emerging markets, price sensitivity limits adoption of premium-priced advanced biologics. Manufacturers must continually demonstrate both clinical efficacy and cost-effectiveness to justify premium pricing in an increasingly cost-conscious global healthcare system.

• Regulatory fragmentation and compliance burdens: The global biosurgery market faces significant challenges from regulatory fragmentation and varying compliance standards across regions. The European Medical Device Regulation (MDR) requires more rigorous clinical evidence and stricter post-market surveillance, creating barriers for both established players and emerging competitors. Asia-Pacific's diverse regulatory landscape presents compliance burdens across China's NMPA, Japan's PMDA, India's CDSCO, and Southeast Asian authorities. Latin America's regulatory fragmentation across ANVISA (Brazil), ANMAT (Argentina), and INVIMA (Colombia) increases time-to-market and compliance costs. The Middle East and Africa's evolving regulatory frameworks, including SAHPRA in South Africa and SFDA in Saudi Arabia, add further complexity.

• Healthcare workforce constraints and infrastructure gaps: Despite significant healthcare investment globally, workforce challenges impact surgical capacity across multiple regions. India requires approximately 291,824 additional surgeons by 2030 to meet demand. South Korea experienced a 4.7% decrease in practicing physicians in 2024. Only the Western Cape in South Africa meets the minimum threshold of 20 surgical specialists per 100,000 population required for safe surgery. Hospital bed density varies widely, from India's 1 bed per 1,000 population to Japan's 8,060 hospitals. Sub-Saharan African governments spend on average only 2% of GDP on health, limiting surgical infrastructure and biosurgical product adoption. Market Trends

• Accelerating shift to ambulatory surgical centers and outpatient settings: The global biosurgery market is undergoing a fundamental structural transformation as surgical care continues its long-term migration from inpatient hospitals to ambulatory surgical centers (ASCs) and outpatient settings. In the United States, there are 12,294 ASCs operating nationwide as of Q2 2025, with procedure volumes forecast to climb 21% during the 2025–2035 window. In the United Kingdom, elective surgical hubs performed 385,482 (14.1%) elective procedures in 2024-25. This shift is driven by technological advances enabling more complex procedures to be performed safely in outpatient settings, patient preference for convenience, and payer initiatives to reduce healthcare expenditure. For biosurgery manufacturers, this trend requires adaptation of product portfolios developing formulations and delivery systems optimized for the fast-paced, high-throughput ASC environment and adjustment of commercial strategies to target the growing ASC customer base.

• Accelerating adoption of robotic-assisted and minimally invasive surgery: Healthcare systems globally are rapidly adopting robotic-assisted and minimally invasive surgical techniques. China's public hospitals procured 84 robotic surgical systems in 2025. Japan's NCD data shows significant growth in laparoscopic procedures, with 120,625 laparoscopic cholecystectomies in 2024. South Korea's minimally invasive surgery market is expected to grow at a CAGR of 7.9% from 2025 to 2033. Saudi Arabia's King Faisal Specialist Hospital performed the world's first fully robotic heart transplant. The Middle East minimally invasive surgery market is expected to grow from USD 7.37–7.80 billion in 2025 to USD 13.41 billion by 2033. This shift creates new opportunities for biosurgical products specifically designed for robotic and minimally invasive applications.

• Growing domestic manufacturing and import substitution initiatives: Governments across major markets are promoting domestic manufacturing of medical devices to reduce import dependence and build local capabilities. China's NMPA registered 3,400 medical device names in 2025, with approximately 40% developed and produced in China. India's medical devices exports reached USD 4.1 billion in FY25, with the industry projected to reach USD 50.1 billion by 2030. Brazil's medical device market is among the top 15 globally, with local manufacturers gaining share. Saudi Arabia's Vision 2030 includes localization targets for medical device manufacturing. These initiatives create opportunities for domestic biosurgery manufacturers while also presenting competitive challenges for international players.
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BiosurgerySegmentation

By Product Bone-Graft Substitutes
Hemostatic Agents
Surgical Sealants & Adhesives
Adhesion Barriers
Soft-Tissue Attachments
Staple-Line Reinforcement
By Application: Orthopedic Surgery
General Surgery
Neurological Surgery
Cardiovascular Surgery
Reconstructive Surgery
Gynecological Surgery
Urological Surgery
Other surgeries (Thoracic surgeries & more)
By Source/Origin Biologic
Synthetic / Semi-synthetic
By End-user: Hospitals
Ambulatory Surgical Centers
Clinics
Others
North America
North America
North America
North America
Europe
Europe
Europe
Europe
Europe
Europe
Europe
Asia-Pacific
Asia-Pacific
Asia-Pacific
Asia-Pacific
Asia-Pacific
Asia-Pacific
South America
South America
South America
South America
MEA
MEA
MEA
MEA



Surgical Sealants and Adhesives is the fastest-growing product segment because increasing adoption of minimally invasive and robotic surgical techniques across all regions creates global demand for advanced tissue-sealing solutions that can be delivered through small incisions.

Surgical Sealants and Adhesives represent the fastest-growing product category in the global biosurgery market, driven by the accelerating adoption of minimally invasive and robotic surgical techniques across all regions. These products including fibrin sealants, synthetic polymer-based sealants, and protein-based adhesives are used to seal tissue surfaces, prevent fluid and air leaks, and reinforce surgical anastomoses. China's public hospitals procured 84 robotic surgical systems in 2025, while Japan's NCD data shows significant growth in laparoscopic procedures, with 120,625 laparoscopic cholecystectomies in 2024. South Korea's minimally invasive surgery market is expected to grow at a CAGR of 7.9% from 2025 to 2033. The Middle East minimally invasive surgery market is expected to grow at a CAGR of 7.02%. This shift toward advanced surgical platforms creates new opportunities for surgical sealants and adhesives that can be delivered through small incisions. Continuous product innovation, including synthetic sealants with enhanced wet-tissue adhesion and faster polymerization times, is expanding the addressable market and creating new clinical applications across cardiovascular, general, and thoracic surgeries. North America leads in the adoption of these advanced technologies, while Asia-Pacific represents the fastest-growing market for surgical sealants and adhesives.

Cardiovascular Surgery is the fastest-growing application segment because rising global cardiovascular disease prevalence, aging populations, and technological advancements in cardiac procedures are increasing worldwide demand for vascular sealants, hemostatic agents, and soft-tissue attachments.

Cardiovascular Surgery represents the fastest-growing application area in the global biosurgery market, driven by the high prevalence of cardiovascular disease and the aging population. Cardiovascular diseases account for approximately 17.9 million deaths annually, representing 32% of all global deaths. China has over 330 million cardiovascular disease patients, with coronary stent procedures expected to reach 2.5 million in 2025. Japan recorded 151,470 cardiovascular surgical procedures in 2024. In the United States, nearly 6.7 million adults are living with heart failure, with the number projected to exceed 8 million by 2030. Vascular sealants, hemostatic agents, and soft-tissue attachments are increasingly utilized in cardiac and vascular procedures, including coronary artery bypass grafting, valve replacements, and vascular reconstructions. The growing adoption of minimally invasive cardiac surgery techniques across all regions is creating new opportunities for advanced biosurgical products designed for smaller incisions and precision delivery. Technological innovations, including synthetic sealants with enhanced adhesion and hemostatic agents with faster action times, are expanding the addressable market and driving adoption across cardiac surgery centers worldwide.

Synthetic and Semi-Synthetic products are the fastest-growing source category because cost-effectiveness, consistent quality, lower immunogenicity risks, and growing domestic manufacturing capabilities support adoption across price-sensitive healthcare markets globally.

Synthetic and Semi-Synthetic products represent the fastest-growing source category in the global biosurgery market, driven by cost-effectiveness, consistent quality, lower immunogenicity risks, and rapidly expanding domestic manufacturing capabilities. These products include synthetic bone substitutes, PEG-based sealants, synthetic meshes, and polysaccharide hemostats. The growing emphasis on cost-containment in healthcare systems globally favors synthetic alternatives for certain applications. China's NMPA approved magnesium-containing biodegradable bone repair materials in 2025, while India's National Medical Devices Policy, 2023, aims to establish the country as a global manufacturing hub for medical devices. The emphasis on cost-effectiveness in healthcare systems, combined with consistent quality and reduced immunogenicity risks, supports the growing adoption of synthetic alternatives across all regions. Asia-Pacific is expected to witness the fastest growth in synthetic biosurgical products, driven by cost sensitivity and growing domestic manufacturing capabilities.

Ambulatory Surgical Centers are the fastest-growing end-user segment because the global shift toward outpatient and same-day discharge models, cost-efficiency, and technological advancements are increasing procedure volumes in ASC settings worldwide.

Ambulatory Surgical Centers (ASCs) represent the fastest-growing end-user segment in the global biosurgery market, driven by the broader healthcare industry shift toward outpatient and same-day discharge models. In the United States, there are 12,294 ASCs operating nationwide as of Q2 2025, with procedure volumes forecast to climb 21% during the 2025–2035 window. In the United Kingdom, elective surgical hubs performed 385,482 (14.1%) elective procedures in 2024-25. Technological advances enabling more complex procedures to be performed safely in outpatient settings, patient preference for convenience, and payer initiatives to reduce healthcare expenditure are driving ASC growth globally. For biosurgery manufacturers, this trend requires adaptation of product portfolios developing formulations and delivery systems optimized for the fast-paced, high-throughput ASC environment and adjustment of commercial strategies to target the growing ASC customer base. North America leads in ASC-based biosurgical product adoption, while Asia-Pacific and Europe are rapidly expanding their outpatient surgical capacity.

Biosurgery Market Regional Insights


North America dominates the global biosurgery market because advanced healthcare infrastructure, high surgical procedure volumes, robust reimbursement systems, and the presence of key market players support widespread biosurgical product utilization.

North America represents the largest regional biosurgery market, driven by its advanced healthcare ecosystem, high surgical volumes, and strong presence of global medical device manufacturers. The United States alone performs approximately 40 million to 50 million major surgical procedures annually, with over a million total joint arthroplasties and more than 400,000 spinal fusion procedures performed each year. Canada's healthcare system provides universal coverage, with provincial health authorities managing hospital budgets and procurement decisions. The region benefits from established reimbursement mechanisms through CMS and private insurers in the United States, widespread availability of specialized surgical centers, and strong adoption of guideline-based treatment pathways. North America accounts for approximately 44.36% of the global biosurgery market, with the United States representing 87.42% of the regional share. Continuous innovation in biosurgery technologies, including advanced hemostatic agents, synthetic sealants, and bioactive bone grafts, is further supporting market expansion. The region is expected to retain its dominant position in the global biosurgery market during the forecast period.
Asia-Pacific is the fastest-growing region because massive surgical volumes, rapid healthcare infrastructure expansion, aging populations, and government policies promoting domestic manufacturing are driving accelerated biosurgery market development.

Asia-Pacific represents the fastest-growing biosurgery market globally, driven by the region's massive surgical volumes, rapid healthcare infrastructure expansion, and large aging populations. China leads with 97.68 million inpatient surgical procedures in 2024 and healthcare expenditure of 9.2 trillion yuan (6.8% of GDP). India performs an estimated 30 million surgeries annually, with the medical devices industry projected to reach USD 50.1 billion by 2030. Japan has the highest proportion of elderly population globally at 29.4% (36.19 million people aged 65 and older). South Korea has officially become a "super-aged society" with 20.7% of its population (10.72 million people) aged 65 and older. Australia recorded 12.8 million hospitalisations in 2024–25. The region accounts for approximately 29.90% of the global biosurgery market. Regulatory modernization across the region, including China's NMPA innovative device review process, Japan's PMD Act amendments, South Korea's Digital Medical Products Act, and India's National Medical Devices Policy, is facilitating faster market access for innovative biosurgical products. Asia-Pacific is expected to maintain the fastest growth rate during the forecast period.
Europe, South America, and the Middle East & Africa contribute significantly to the global biosurgery market with established healthcare systems and expanding surgical capacity.

Europe represents a mature biosurgery market accounting for approximately 19.66% of the global market. Germany leads with 16,531,491 surgical procedures in 2023 and healthcare expenditure of EUR 579.5 billion (12.4% of GDP). France records more than 9 million surgical interventions annually, while the United Kingdom performs 8,251,733 episodes with a procedure in NHS providers in 2025/26. Italy has 24.7% of its population aged 65 and older, the highest median age in the EU at 48.7 years. Spain is the fastest-growing country in the European biosurgery market, with over 10 million people aged 65 and older (20.7% of the population). The European Commission's proposed MDR amendments are expected to facilitate faster market access for innovative biosurgical products. South America accounts for approximately 3.53% of the global biosurgery market, with Brazil leading at 51.96% of the regional share. Brazil performed 14.7 million elective surgeries through SUS in 2025, with the elderly population (60 years and older) reaching 16.6% of the total population. Colombia is the fastest-growing country in the region, having achieved 99% healthcare coverage of its population. The Middle East and Africa represent a small but rapidly growing market, with Saudi Arabia accounting for 35.73% of the regional share and the UAE at 16.01%. Saudi Arabia's Vision 2030 healthcare transformation program includes significant investments in surgical capacity and robotic-assisted surgery. The Middle East minimally invasive surgery market is expected to grow at a CAGR of 7.02%. South Africa is the largest biosurgery market in Sub-Saharan Africa, with health spending reaching 9.14% of GDP in 2025.

Key Developments


• July 2026: EQT agreed to acquire Corza Biosurgery, the manufacturer of TachoSil®, a leading hemostatic and sealing patch, from Corza Medical.
The transaction is expected to close during Q4 2026, with EQT planning to invest in commercial acceleration and geographic expansion.

• April 2026: BIOTRONIK announced U.
S.
FDA approval for its Acticor Sky and Rivacor Sky implantable cardioverter-defibrillator (ICD) and cardiac resynchronization therapy defibrillator (CRT-D) systems.
The Sky device family expands the company's cardiac rhythm portfolio with technologies designed to support physiology-driven therapies and improve clinical workflows.

• April 2026: Abbott presented four late-breaking clinical studies at the Heart Rhythm Society (HRS) 2026 meeting in Chicago, highlighting clinical evidence across its pulsed field ablation technologies and novel cardiac pacing portfolio, including conduction system pacing innovations.

• March 2026: Medtronic received U.
S.
FDA approval for an expanded indication of its OmniaSecure™ defibrillation lead, allowing placement in the left bundle branch area for conduction system pacing when connected to ICD or CRT-D systems.

• February 2026: BIOTRONIK launched the Acticor Sky and Rivacor Sky device family across CE markets, introducing the world's first CE-approved high-voltage device supporting left bundle branch area pacing (LBBAP) within ICD and CRT-D systems.

• December 2025: Solventum completed the acquisition of Acera Surgical, a privately held bioscience company focused on developing engineered materials for regenerative wound care.
The acquisition expands Solventum's MedSurg portfolio into the synthetic tissue matrices technology space in acute care settings.

• December 2025: The FDA cleared TRAUMAGEL® 2.
0 Hemostatic Gel (K253609), a hemostatic gel indicated for temporary external use for controlling moderate to severe bleeding.

• December 2025: The FDA cleared MFUSE™, a sterile, single-use, disposable hemostatic hydrogel paste for temporary external use for controlling moderate to severe bleeding.

• November 2025: The FDA cleared XSTAT P15 (K253290), a hemostatic wound dressing for emergency trauma control.

• September 2025: The FDA cleared FG Bone Graft M (K244006), intended for use as a bone grafting material to fill, augment or reconstruct periodontal or oral/maxillofacial defects.

• September 2025: Baxter's Preveleak Surgical Sealant received FDA PMA supplement approval (P100030 S021).

• August 2025: The FDA cleared FG Bone Graft B (K243745).

• July 2025: The FDA approved SURGIFLO® Hemostatic Matrix, an absorbable hemostatic agent.

• July 2025: Zimmer Biomet announced a definitive agreement to acquire Monogram Technologies, expanding its robotics suite with autonomous solutions.
The acquisition is expected to be neutral to adjusted earnings per share in 2025–2027 and accretive thereafter.

• June 2025: Cerapedics Inc.
received FDA premarket approval for its PearlMatrix™ P-15 Peptide Enhanced Bone Graft, the first and only bone growth accelerator proven to accelerate lumbar fusion based on data from the pivotal ASPIRE IDE study.

• June 2025: Aroa Biosurgery Ltd.
received FDA 510(k) clearance for Endoform™ Reconstructive Template – PLGA, intended for use as a surgical mesh to reinforce and/or repair soft tissue where weakness exists.

• June 2025: The FDA cleared Grafton™ DBM (K251193).

• May 2025: Johnson & Johnson MedTech announced the U.
S.
introduction of MENTOR™ MemoryGel™ Enhance Breast Implants, addressing a vital need in complete breast cancer treatment for women who have had a mastectomy.

• May 2025: Baxter introduced Hemopatch Sealing Hemostat, a collagen-based pad featuring a dual-action system that merges a collagen matrix with a reactive NHS-PEG coating for enhanced hemostatic capabilities.
The revised formulation permits storage at room temperature and extends shelf life to three years.

• April 2025: Restor3D, a firm focused on 3D-printed, custom orthopedic implants, secured $38 million in growth funding to accelerate its expansion and introduce four new product lines over the next two years, including the Veritas shoulder, iTotal Identity knee, Kinos ankle, and Velora hip cup.

• April 2025: simAbs opened a new GMP cleanroom facility in collaboration with Sealantium Medical, a biosurgery enterprise dedicated to creating next-generation tissue sealants and hemostatic agents for surgical patients.

• April 2025: The U.
S.
FDA granted Premarket Approval (PMA) for the WiSE CRT System, the world's first leadless left ventricular endocardial pacing system for cardiac resynchronization therapy (CRT), enabling leadless LV pacing for eligible heart failure patients.

• April 2025: Ventris Medical secured additional FDA clearance for Backpack® Bone Graft in intervertebral disc applications.

• March 2025: Olympus announced the introduction of the Retentia™ HemoClip, a new hemostasis clip featuring 360° rotation and a user-friendly one-step deployment, available in three sizes to suit various closure needs.

• March 2025: Teleflex announced a definitive agreement to acquire substantially all of BIOTRONIK's Vascular Intervention business for approximately €760 million in cash.

• March 2025: The FDA cleared QuikClot Control+ Hemostatic Device (K243553).

• February 2025: The FDA cleared Synthetic Bone Graft Particulate (K241186).

• February 2025: The FDA cleared Resolution Clip (K250066).

• January 2025: Kuros Biosciences USA, Inc.
entered into an exclusive strategic agreement with Medtronic's Spinal Division, appointing Medtronic as the exclusive sales agent for MagnetOs in designated territories for spinal surgery applications.

• January 2025: Royal Biologics signed an exclusive distribution agreement with Aroa Biosurgery for Myriad Matrix™ Restore, expanding access to advanced soft tissue repair solutions across outpatient and mobile care settings in the U.
S.

• January 2025: Aroa Biosurgery published additional robust clinical evidence supporting both the effectiveness and cost advantages of its AROA ECM™ technology in high-risk limb salvage surgery.
The single-site prospective clinical study involved 130 complex lower limb defects from 120 patients, with 95% of participants having at least one risk factor for lower limb amputation.

• January 2025: The FDA expanded the indication of ARTISS for use in adult and pediatric patients to adhere autologous skin grafts to surgically prepared wound beds resulting from burns and to adhere tissue flaps during facial rhytidectomy surgery.

• January 2025: The FDA expanded the indication of TISSEEL for use in adult and pediatric patients as an adjunct to hemostasis and to prevent leakage from colonic anastomoses following the reversal of temporary colostomies.
May 2023: BIOTRONIK received CE approval for the Amvia Sky and Amvia Edge pacemaker family, including CRT-P models approved for left bundle branch area pacing (LBBAP), expanding support for physiologic pacing therapies.

Companies Mentioned

  • 1 . Johnson & Johnson,
  • 2 . Baxter International Inc.
  • 3 . Medtronic plc
  • 4 . Becton, Dickinson and Company
  • 5 . B. Braun Melsungen AG
  • 6 . Integra LifeSciences
  • 7 . Stryker corporation
  • 8 . Zimmer Biomet Holdings, Inc.
  • 9 . Artivion, Inc.
  • 10 . Smith & Nephew plc
Company mentioned

Table of Contents

  • Table 1: Global Bio surgery Market Snapshot, By Segmentation (2025 & 2031F) (in USD Billion)
  • Table 2: Influencing Factors for Bio surgery Market, 2025
  • Table 3: Top 10 Counties Economic Snapshot 2024
  • Table 4: Economic Snapshot of Other Prominent Countries 2022
  • Table 5: Average Exchange Rates for Converting Foreign Currencies into U.S. Dollars
  • Table 6: Global Bio surgery Market Size and Forecast, By Geography (2020 to 2031F) (In USD Billion)
  • Table 7: Global Bio surgery Market Size and Forecast, By Product (2020 to 2031F) (In USD Billion)
  • Table 8: Global Bio surgery Market Size and Forecast, By Source (2020 to 2031F) (In USD Billion)
  • Table 9: Global Bio surgery Market Size and Forecast, By Application (2020 to 2031F) (In USD Billion)
  • Table 10: Global Bio surgery Market Size and Forecast, By End-user (2020 to 2031F) (In USD Billion)
  • Table 11: North America Bio surgery Market Size and Forecast, By Product (2020 to 2031F) (In USD Billion)
  • Table 12: North America Bio surgery Market Size and Forecast, By Source (2020 to 2031F) (In USD Billion)
  • Table 13: North America Bio surgery Market Size and Forecast, By Application (2020 to 2031F) (In USD Billion)
  • Table 14: North America Bio surgery Market Size and Forecast, By End-user (2020 to 2031F) (In USD Billion)
  • Table 15: Europe Bio surgery Market Size and Forecast, By Product (2020 to 2031F) (In USD Billion)
  • Table 16: Europe Bio surgery Market Size and Forecast, By Source (2020 to 2031F) (In USD Billion)
  • Table 17: Europe Bio surgery Market Size and Forecast, By Application (2020 to 2031F) (In USD Billion)
  • Table 18: Europe Bio surgery Market Size and Forecast, By End-user (2020 to 2031F) (In USD Billion)
  • Table 19: Asia-Pacific Bio surgery Market Size and Forecast, By Product (2020 to 2031F) (In USD Billion)
  • Table 20: Asia-Pacific Bio surgery Market Size and Forecast, By Source (2020 to 2031F) (In USD Billion)
  • Table 21: Asia-Pacific Bio surgery Market Size and Forecast, By Application (2020 to 2031F) (In USD Billion)
  • Table 22: Asia-Pacific Bio surgery Market Size and Forecast, By End-user (2020 to 2031F) (In USD Billion)
  • Table 23: South America Bio surgery Market Size and Forecast, By Product (2020 to 2031F) (In USD Billion)
  • Table 24: South America Bio surgery Market Size and Forecast, By Source (2020 to 2031F) (In USD Billion)
  • Table 25: South America Bio surgery Market Size and Forecast, By Application (2020 to 2031F) (In USD Billion)
  • Table 26: South America Bio surgery Market Size and Forecast, By End-user (2020 to 2031F) (In USD Billion)
  • Table 27: Middle East & Africa Bio surgery Market Size and Forecast, By Product (2020 to 2031F) (In USD Billion)
  • Table 28: Middle East & Africa Bio surgery Market Size and Forecast, By Source (2020 to 2031F) (In USD Billion)
  • Table 29: Middle East & Africa Bio surgery Market Size and Forecast, By Application (2020 to 2031F) (In USD Billion)
  • Table 30: Middle East & Africa Bio surgery Market Size and Forecast, By End-user (2020 to 2031F) (In USD Billion)
  • Table 31: Competitive Dashboard of top 5 players, 2025
  • Table 32: Key Players Market Share Insights and Analysis for Bio surgery Market 2025

  • Figure 1: Global Bio surgery Market Size (USD Billion) By Region, 2025 & 2031F
  • Figure 2: Market attractiveness Index, By Region 2031F
  • Figure 3: Market attractiveness Index, By Segment 2031F
  • Figure 4: Global Bio surgery Market Size By Value (2020, 2025 & 2031F) (in USD Billion)
  • Figure 5: Global Bio surgery Market Share By Region (2025)
  • Figure 6: North America Bio surgery Market Size By Value (2020, 2025 & 2031F) (in USD Billion)
  • Figure 7: North America Bio surgery Market Share By Country (2025)
  • Figure 8: Europe Bio surgery Market Size By Value (2020, 2025 & 2031F) (in USD Billion)
  • Figure 9: Europe Bio surgery Market Share By Country (2025)
  • Figure 10: Asia-Pacific Bio surgery Market Size By Value (2020, 2025 & 2031F) (in USD Billion)
  • Figure 11: Asia-Pacific Bio surgery Market Share By Country (2025)
  • Figure 12: South America Bio surgery Market Size By Value (2020, 2025 & 2031F) (in USD Billion)
  • Figure 13: South America Bio surgery Market Share By Country (2025)
  • Figure 14: Middle East & Africa Bio surgery Market Size By Value (2020, 2025 & 2031F) (in USD Billion)
  • Figure 15: Middle East & Africa Bio surgery Market Share By Country (2025)
  • Figure 16: Porter's Five Forces of Global Bio surgery Market

Biosurgery Market Research FAQs

The global biosurgery market is expected to cross USD 25.08 Billion by 2031, growing at a CAGR of 6.13% from 2026 to 2031. Growth is supported by rising surgical volumes, aging populations, advanced hospitals, reimbursement support, and continuous product innovation in surgical biomaterials across all regions.
North America dominates the global biosurgery market, driven by its advanced healthcare infrastructure, high surgical procedure volumes, robust reimbursement systems, and the presence of key market players. North America accounts for approximately 44.36% of the global market.
Asia-Pacific is the fastest-growing region in the global biosurgery market, driven by massive surgical volumes, rapid healthcare infrastructure expansion, aging populations, and government policies promoting domestic manufacturing.
Bone-Graft Substitutes represent the largest product category in the global biosurgery market, driven by the high volume of spinal fusion procedures, joint replacements, and orthopedic trauma surgeries across all regions.
Surgical Sealants and Adhesives represent the fastest-growing product category, driven by increasing adoption of minimally invasive and robotic surgical techniques across all healthcare systems globally.
Orthopedic Surgery is the largest application area for biosurgical products globally, driven by the high volume of joint replacements, spinal fusions, and trauma procedures across all regions.
Cardiovascular Surgery is growing fastest due to high prevalence of cardiovascular disease, aging populations, and technological advancements in cardiac procedures across all regions.
Future biosurgery growth will be influenced by regulatory modernization, robotic-assisted surgery adoption, minimally invasive surgical techniques, personalized surgical approaches, and next-generation synthetic biomaterials developed by manufacturers across all regions.

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