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A Detailed Analysis of the Market for Hernia Mesh Devices Based on an Expanding Aging Population, a Surge in Hernia Repair Procedures, and Technological Advancements
The global hernia mesh devices market is forecast to expand at a CAGR of 6.9% and thereby increase from a value of US$5.3 Bn in 2023, to US$8.5 Bn by the end of 2030.
Hernia Mesh Devices Market Size (2023E)
Projected Market Value (2030F)
Global Market Growth Rate (CAGR 2023 to 2030)
Historical Market Growth Rate (CAGR 2018 to 2022)
The global market for hernia mesh devices is being propelled by the rising incidence of hernias, which has generated a need for surgical solutions that are both efficient and long-lasting. Hernias, which manifest as the protrusion of organs or tissues through compromised regions of the abdominal wall, is a prevalent medical condition. An increasing number of sedentary occupations, aging populations, and obesity rates are all contributing factors to the global increase in hernia incidence. The abdominal wall's connective tissues tend to deteriorate with age, rendering them more vulnerable to hernias.
Additional significant factors include the prevalence of obesity, given that both abdominal pressure and superfluous weight elevate the likelihood of developing hernias. Sedentary behaviors, which consist of insufficient physical activity, additionally exacerbate the vulnerability of abdominal muscles, thereby increasing the likelihood that an individual will develop a hernia. The rising incidence of hernias has prompted an upsurge in the quantity of hernia repair operations, thereby propelling the need for hernia mesh devices.
In the absence of mesh, conventional hernia closure techniques were linked to increased recurrence rates, prolonged recovery periods, and postoperative complications. By offering a more robust and long-lasting alternative, hernia repair surgeries have been transformed since the introduction of hernia mesh devices. By providing structural support to the compromised abdominal wall, mesh devices decrease the likelihood of hernia recurrence and expedite the recovery process for the patient. With the increasing recognition of the advantages associated with hernia mesh surgeries among healthcare professionals and patients alike, there is a growing inclination towards these procedures in comparison to conventional approaches.
There is a substantial increase in hernia repair surgeries globally, owing to a rising prevalence of hernias and the aging population. The demand for minimally invasive procedures has fueled the adoption of hernia mesh devices, as they offer quicker recovery and reduced postoperative complications. Technological advancements in mesh materials and designs contribute to improved patient outcomes, enhancing the market's attractiveness. Additionally, the growing awareness among healthcare professionals and patients regarding the benefits of mesh repair over traditional methods further propels market expansion.
Hernia mesh devices are in high demand for the critical nature of patient safety. To stop the transmission of infections and eradicate pathogenic microorganisms, medical devices, surgical instruments, and healthcare hernia types must be subjected to rigorous sterilization processes. The proliferation of healthcare facilities worldwide has generated a growing demand for reliable sterilization techniques, which has propelled the implementation of hernia mesh devices.
Additionally, to ensure the safety and efficacy of its hernia types, the pharmaceutical industry, which manufactures a vast array of medications and medical supplies, employs rigorous sterilization procedures. In the pursuit of regulatory compliance and hernia type quality assurance, pharmaceutical companies are increasingly turning to irradiation sterilization as a preferred technique. This is primarily due to the method's capacity to permeate packaging materials without imparting residues or modifying the composition of delicate pharmaceutical compounds.
Complexities, and Concerns Around the Same
Expanding litigation and apprehensions regarding complications linked to certain mesh products are a factor restraining the global market for hernia mesh devices. Complications including infections, chronic pain, adhesion formation, and mesh migration have been associated with specific hernia mesh devices over time. Concerns regarding the safety of hernia mesh implants have been raised by healthcare providers and patients due to the rise in litigation filed against manufacturers in response to adverse event and complication reports.
Responses from regulatory bodies and heightened vigilance among medical professionals have been prompted by the scrutiny surrounding complications associated with hernia mesh. Concerned healthcare professionals have been compelled to reconsider their selections of mesh products in the light of safety communications and warnings issued by regulatory agencies.
Growing Regulatory Scrutiny
An influential factor affecting the worldwide market for hernia mesh devices is the escalating regulatory scrutiny and apprehensions regarding the safety of specific mesh products. In the light of documented complications, regulatory bodies have intensified their surveillance of the safety profiles of hernia mesh devices. The increased scrutiny surrounding mesh products has resulted in more stringent regulations, safety advisories, and product recalls.
Manufacturers are thus confronted with obstacles concerning market entry and adherence to regulations. The regulatory framework pertaining to hernia mesh devices has undergone increased scrutiny due to the emergence of concerns regarding complications such as chronic pain, infections, and mesh migration. Manufacturers encounter the formidable task of satisfying ever-changing regulatory standards while also providing substantial clinical evidence of the safety and effectiveness of their products.
Continuous Advancements in Sophisticated Mesh Technologies
An opportunistic factor propelling the worldwide market for hernia mesh devices is the ongoing development and innovation of sophisticated mesh technologies. Manufacturers are increasing their investments in research and development to produce mesh devices that exhibit improved patient outcomes, decreased complications, and enhanced biocompatibility as technology advances. Biological and absorbable meshes, among other advanced materials, are becoming increasingly prominent in the marketplace. By progressively being absorbed by the body over time, absorbable meshes reduce the risk of long-term complications and eliminate the need for permanent implantation. By virtue of being derived from human or animal tissues, biologic scaffolds intend to render hernia repair a more organic and unified process.
The advancement of minimally invasive surgical techniques constitutes an additional facet of technological innovation that propels the market for hernia mesh devices. The prevalence of laparoscopic and robotic-assisted hernia repair procedures has increased due to their advantageous characteristics, including reduced pain, shorter recuperation times, smaller incisions, and decreased postoperative complications. The introduction of mesh devices tailored for these minimally invasive procedures is an additional factor driving market expansion. These advancements not only enhance the overall effectiveness of hernia repair but also mitigate issues linked to conventional open surgeries, thereby expanding the treatment options for patients and healthcare practitioners to include personalized and efficient interventions.
The global market for hernia mesh devices is anticipated to experience significant expansion due to a confluence of factors including shifting healthcare environments, technological progress, and demographic shifts. An influential factor driving market expansion is the escalating incidence of hernias on a global scale. An increasing number of sedentary lifestyles, aging populations, and rising obesity rates all contribute to the rising incidence of hernias, which necessitates the development of effective and long-lasting hernia repair methods.
The increasing demand for hernia mesh devices is anticipated to drive market growth, particularly in regions such as South Asia, and the Pacific, and North America, where there is a heightened awareness of healthcare and a rising volume of surgical procedures. The dynamic between manufacturers and consumers in the market for hernia mesh devices is of paramount importance as it significantly influences the course of the industry.
There is a growing emphasis among manufacturers on research and development to advance and enhance mesh technologies. Developing biocompatible materials, minimizing complications, and improving patient outcomes are of the utmost importance. Nevertheless, the market has encountered obstacles because of litigations and safety concerns concerning specific mesh products. To establish and sustain consumer confidence, it is imperative for manufacturers to deal with evolving regulatory standards, prioritize transparency, and conduct rigorous testing.
It is critical to establish a strong feedback loop among manufacturers, healthcare providers, and patients to promptly address concerns and adjust products to meet changing requirements. Moreover, market participants must adeptly navigate regulatory obstacles. Manufacturers are compelled to comply with more stringent regulations and safety advisories to establish the safety and effectiveness of their products through rigorous testing. Maintaining market success requires an ongoing dialogue with regulatory authorities and a proactive stance towards safety concerns.
In summary, the worldwide market for hernia mesh devices offers a favorable environment for producers, as there is an increasing need for inventive approaches to hernia repair. Although this market is dynamic and ever-changing, manufacturers can achieve success by implementing strategic initiatives that prioritize technological advancements, regulatory compliance, and transparent communication, despite the presence of certain obstacles. The partnership among manufacturers, healthcare practitioners, and regulatory agencies will have a critical impact on the trajectory of the hernia mesh devices industry.
On the global market for hernia mesh devices, Medtronic plc, Ethicon (Johnson & Johnson), B. Braun Melsungen AG, W. L. Gore & Associates, and C.R. Bard (a subsidiary of BD) are significant participants. These sector frontrunners are actively engaged in innovative product development, market penetration, and strategic alliances, thereby making substantial contributions to the competitive environment of the market. The US especially emerges as a preeminent region in terms of the adoption of hernia mesh devices.
Prominent surgical techniques, a robust healthcare infrastructure, and a high incidence of hernias all contribute to the market's substantial utilization. Europe is witnessing notable contributions from nations such as Germany, and the UK, propelled by the expansion of the elderly demographic and heightened consciousness regarding inventive hernia repair methodologies. South Asia, and the Pacific, including India, exhibits a rising trend in market utilization due to rising awareness, an improving healthcare infrastructure, and an increase in the number of surgical procedures.
Market leaders are proactively reshaping the terrain by means of ongoing product development and innovation. To illustrate, Medtronic, and Ethicon, a subsidiary of Johnson & Johnson, are allocating resources towards investigating and developing sophisticated mesh materials—including biologic and absorbable meshes—with the objective of enhancing biocompatibility and mitigating complications. Their unwavering commitment to innovation serves to distinguish their products and propels the market in the direction of more effective and user-centric solutions.
Which is the Leading Mesh Type Segment?
Synthetic Mesh Type Takes the Lead for its Longer Durability
It is anticipated that the synthetic mesh segment will hold the highest market share in the market for hernia mesh devices. Synthetic meshes, which are commonly constructed from polypropylene, and other similar materials, are extensively employed in hernia repair procedures on account of their cost-effectiveness, durable nature, and established history of delivering structural support. The segment's dominant market position is a result of the extensive embrace and implementation of synthetic mesh products by healthcare facilities and surgeons.
Although it is expected that the synthetic mesh segment will maintain its dominant market share, the biological mesh segment is projected to experience the most rapid growth. The increasing popularity of biological meshes, which are sourced from animal or human tissues, can be attributed to their capacity to enhance tissue integration, and mitigate long-term complications. The increasing biocompatibility and effectiveness of biological meshes facilitated by technological progress is anticipated to generate a burgeoning market for these novel solutions, thereby propelling the biological mesh sector of the hernia mesh devices industry forward at a rapid rate. This trend signifies a transition towards hernia repair procedures that are more sophisticated and convenient for the patient.
Which Hernia Type is Prominent?
Inguinal Hernia Identified to be the Most Prominent Category
It is anticipated that the inguinal hernia segment will hold the most significant portion of the market for hernia mesh devices. Hernias of the inguinal region are the most prevalent, accounting for a substantial proportion of hernia repair procedures. Consequently, the substantial demand for mesh devices designed for the repair of inguinal hernias contributes to the market dominance observed in this segment. It is expected that the incisional hernia segment will experience the most rapid growth.
As the number of abdominally incision-based surgical procedures increases, so does the incidence of incisional hernias. The anticipated surge in demand for durable and efficacious hernia mesh devices intended for incisional hernia repair will propel the market segment's exponential expansion. In the coming years, technological advancements and an increased recognition of the advantages associated with mesh-based repairs for incisional hernias are anticipated to contribute to the surge in growth of this market segment.
North America Spearheads with a Greater Inclination Towards Novel Medical Technologies
It is anticipated that North America will hold the largest market share of the worldwide hernia mesh devices market. There are multiple factors that contribute to this region's dominant position. To begin with, North America boasts a firmly established healthcare infrastructure, cutting-edge medical facilities, and a notable propensity for rapidly embracing novel medical technologies. Furthermore, the widespread occurrence of hernias, specifically those involving the ingenium and incision, serves as a catalyst for the regional demand for hernia mesh devices.
A further driver of market expansion is the geriatric population in North America, which is associated with a heightened susceptibility to hernias. Additionally, the region's predominance in the hernia mesh devices market is supported by the presence of significant market participants and continuous research and development efforts. The positive reimbursement environment and the recognition of the advantages of mesh-based hernia repair among patients and healthcare professionals are additional factors that significantly contribute to North America's prominence in the international market.
South Asia, and the Pacific Accelerate as Witness Rising Prevalence of Hernias
It is expected that South Asia, and the Pacific will witness the most rapid expansion of the worldwide hernia mesh devices market. Numerous elements within the region are favourable for market expansion. In the first place, the increasing incidence of hernias in South Asia, and the Pacific, which can be attributed to factors such as lifestyle modifications, population expansion, and the rise in surgical procedures, drives the demand for hernia mesh devices.
Furthermore, advancements in healthcare infrastructure, heightened healthcare consciousness, and rising disposable income all play a role in promoting the acceptance and utilization of sophisticated medical technologies, such as hernia mesh devices. It is anticipated that the demand for mesh-based hernia repair devices will increase in tandem with the growing awareness of their advantages. Additionally, the considerable market opportunity for manufacturers is complemented by the region's sizable and diverse population. To fully exploit the growth potential of the hernia management market in South Asia, and the Pacific, it is critical to effectively navigate regulatory frameworks, address healthcare disparities, and promote education on the subject. In general, the confluence of an increasing incidence of hernias and the evolution of the healthcare sector situates this area for substantial and expeditious market expansion.
Seizing a substantial portion of one's market share requires substantial investments in research and development. These businesses pursue innovation on an ongoing basis through the development of cutting-edge materials and technologies for hernia mesh devices. For example, Medtronic and Ethicon have been at the forefront of investigating absorbable and biologic meshes. These advancements are designed to ameliorate safety apprehensions, decrease complications, and enhance biocompatibility in relation to conventional synthetic meshes. These companies distinguish their products in a competitive market and ensure that they continue to address the changing demands of healthcare professionals by remaining at the vanguard of technological developments.
Market leaders frequently form strategic alliances and collaborations as a means of fortifying their market standing. Working with healthcare institutions, research organizations, or other industry stakeholders may be required for these collaborations. These companies, for instance, conduct clinical trials, collect real-world data, and bolster the clinical evidence supporting the efficacy and safety of their products through collaborations with prestigious academic institutions or hospitals. In addition to facilitating market penetration, these strategic alliances grant the involved companies access to a broader consumer base and the ability to develop robust networks.
Ariste Medical, LLC, a pre-commercial drug and device company, disclosed in April 2022 that its drug-embedded synthetic hernia mesh had been granted approval by the US FDA. The mesh was designed to prevent microbial infections that may occur during surgical implantation.
Market Impact: The approval of the drug-embedded synthetic hernia mesh by Ariste Medical, LLC by the FDA signifies a substantial advancement in the international market. By preventing microbial infections during surgical implantation, this innovative product effectively resolves a significant issue that arises during hernia repair procedures. The approval not only signifies progress in mesh technologies but also introduces a potentially transformative innovation that could enhance the safety and effectiveness of hernia repairs on a global scale. This could have an impact on the market by establishing a new benchmark for infection prevention in hernia mesh devices.
2023 to 2030
Historical Data Available for
2018 to 2022
US$ Million for Value
Key Regions Covered
Key Countries Covered
Key Market Segments Covered
Key Companies Profiled
Customization & Pricing
Available upon request
By Mesh Type:
By Hernia Type:
The market is anticipated to grow at a CAGR of 6.9% during the projected period.
The hernia mesh devices market was valued at US$5.3 billion in 2023.
The US held the largest market share in 2023.
Some of the prominent players in the market are Medtronic Plc, Ethicon, W. L. Gore and Associates, Inc, and Atrium Medical Technologies.
The incisional hernia segment is expected to witness the fastest CAGR during the forecast period.