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市場調查報告書
商品編碼
1797995
2032 年神經調節設備市場預測:按產品類型、適應症、MRI 相容性、生醫材料、最終用戶和地區進行的全球分析Neuromodulation Devices Market Forecasts to 2032 - Global Analysis By Product Type, Indication, MRI Compatibility, Biomaterial, End User and By Geography |
根據 Stratistics MRC 的數據,全球神經調節設備市場預計在 2025 年達到 22 億美元,到 2032 年將達到 120 億美元,預測期內的複合年成長率為 5.0%。
神經調節裝置是一種醫療技術,旨在透過向特定神經或神經部位傳遞定向刺激(例如電脈衝或化學藥劑)來改變神經活動。這些裝置通常用於糾正異常神經訊號,以恢復或使神經系統功能正常化,並緩解慢性疼痛、運動障礙和神經功能障礙等症狀。刺激透過調節神經興奮性和通路,直接影響神經傳遞,進而產生治療效果。
根據美國癲癇基金會和世界衛生組織 (WHO) 的數據,全球約有 5,000 萬人患有癲癇。
慢性神經系統疾病的增加
帕金森氏症、癲癇、阿茲海默症和慢性疼痛症候群等神經系統疾病的盛行率不斷上升,是神經調節設備市場的主要驅動力。人口老化和生活方式相關併發症的增多,推動了對微創、長期治療方案的需求。神經調節設備提供有針對性的、可逆的、可程式設計的治療方案,使其成為一種頗具吸引力的藥物替代方案。神經系統疾病負擔的日益加重,促使醫療保健系統和從業人員採用此類創新治療方法。
神經調節劑高成本
神經調節裝置相關的高昂成本(包括植入、維護和編程)構成了其廣泛應用的重大障礙。高昂的初始投資,加上某些地區的報銷額度有限,限制了其普及,尤其是在中低收入國家。此外,後續觀察、電池更換和設備相關服務進一步增加了長期治療成本。這些經濟限制限制了嚴重患者的應用,並延誤了缺乏足夠保險或政府支持的患者的治療。
神經調節療法的認知度和接受度不斷提高
人們對非藥物疼痛和神經系統治療的認知日益加深,使得患者和醫護人員對神經調節療法的接受度不斷提高。教育宣傳活動、臨床成功案例以及不斷擴展的臨床證據增強了人們對基於設備的治療方法的信心。此外,個人化醫療和精準醫療的轉變也增強了神經調節療法的吸引力。隨著圍繞植入式設備的污名逐漸消退,以及該技術越來越普及,新的患者群體正在進入市場,尤其是在先前缺乏先進神經介入療法服務的地區。
設備相關併發症和副作用的風險
感染疾病、導線移位、硬體故障以及刺激相關副作用等潛在風險仍令人擔憂,威脅市場擴張。這些併發症可能導致設備再次手術或移除,增加患者不適感和治療成本。此外,對手術植入、長期依賴性以及對其他身體系統的潛在干擾的擔憂,也令患者和醫生感到沮喪。負面結果和備受矚目的產品召回也可能影響大眾對神經調節技術的信任。
由於封鎖措施以及資源向重症監護的重新分配,COVID-19 疫情最初擾亂了擇期神經調節手術。許多患者推遲了手術,導致銷售額和植入數量在短期內下降。然而,疫情後的復甦得益於對慢性病管理的重新關注以及門診治療需求的增加。遠端醫療和遠端設備編程解決方案也已成為寶貴的工具,確保了護理的連續性,並重塑了神經調節領域的服務交付模式。
脊髓刺激設備市場預計將成為預測期內最大的市場
預計脊髓刺激設備細分市場將在預測期內佔據最大市場佔有率,這主要得益於慢性腰腿痛的高發生率。這些裝置廣泛用於治療腰椎手術失敗症候群和複雜性局部疼痛症候群,並已證明其長期療效。閉合迴路系統和無線編程等持續的產品創新正在改善治療效果和患者依從性。此外,主要市場的優惠報銷政策也進一步推動了脊髓刺激設備的大規模應用。
深層腦部刺激器領域預計將在預測期內實現最高複合年成長率
預計深層腦部刺激器領域將在預測期內呈現最高成長率,這得益於對治療帕金森氏症、肌張力不全症和自發性震顫等先進療法的需求不斷成長。精準定位和程式靈活性方面的技術進步正在改善患者的治療效果。此外,在憂鬱症和強迫性精神官能症精神疾病和神經精神疾病應用方面的研究日益增多,也正在擴大深部腦部刺激的應用範圍。隨著臨床適應症的擴展,該領域有望加速全球成長。
預計亞太地區將在預測期內佔據最大市場佔有率,這得益於神經系統疾病盛行率上升、醫療支出增加以及先進醫療技術日益普及等因素。中國、日本和印度等國家正在大力投資神經病學基礎設施和基於設備的治療。此外,患者意識的增強、私人醫療網路的擴張以及政府在神經復健領域的扶持政策正在推動區域需求。龐大的人口規模和日益加速的都市化進一步鞏固了亞太地區在神經調節設備市場的主導地位。
預計北美地區在預測期內將實現最高的複合年成長率,這得益於神經病變率的上升、醫療保健支出的增加以及先進醫療技術的普及。中國、日本和印度等國家正在大力投資神經病學基礎設施和基於設備的療法。此外,患者意識的增強、私人醫療網路的擴張以及政府對神經復健的支持也推動了區域需求。龐大的人口和日益加速的都市化進一步鞏固了亞太地區在神經調節設備市場的主導地位。
According to Stratistics MRC, the Global Neuromodulation Devices Market is accounted for $2.2 billion in 2025 and is expected to reach $12.0 billion by 2032 growing at a CAGR of 5.0% during the forecast period. Neuromodulation devices are medical technologies designed to alter nerve activity by delivering targeted stimuli, such as electrical impulses or chemical agents, to specific nerves or neurological sites. These devices modify abnormal nerve signals to restore or normalize nervous system functions, often used to relieve symptoms like chronic pain, movement disorders, or neurological dysfunctions. The stimulation can adjust nerve excitability or pathways, providing therapeutic effects by influencing nerve communication directly.
According to the Epilepsy Foundation of America and World Health Organization (WHO), an estimated 50 million people globally were suffering from epilepsy.
Increasing prevalence of chronic neurological diseases
The growing incidence of neurological disorders such as Parkinson's disease, epilepsy, Alzheimer's, and chronic pain syndromes is a key driver for the neuromodulation devices market. With aging populations and lifestyle-related complications on the rise, demand for minimally invasive, long-term therapeutic solutions is increasing. Neuromodulation devices offer targeted, reversible, and programmable therapy, making them attractive alternatives to pharmaceuticals. The rising burden of neurological conditions is pushing healthcare systems and practitioners to adopt these innovative treatment modalities.
High cost of neuromodulation devices
The significant cost associated with neuromodulation devices, including implantation, maintenance, and programming, poses a major barrier to widespread adoption. High initial investment, coupled with limited reimbursement coverage in several regions, restricts access, especially in low- and middle-income countries. Additionally, follow-up visits, battery replacements, and device-related services further inflate long-term treatment costs. These economic limitations discourage adoption in non-critical cases and delay therapy for patients without sufficient insurance or government support.
Growing awareness and acceptance of neuromodulation therapies
Increased awareness of non-pharmacological pain and neurological treatments has led to rising acceptance of neuromodulation therapies across both patients and healthcare providers. Educational campaigns, clinical success stories, and expanding clinical evidence are building trust in device-based therapies. Furthermore, the shift toward personalized and precision medicine supports neuromodulation's appeal. As stigma around implantable devices decreases and technology becomes more accessible, new patient demographics are entering the market, especially in regions previously underserved by advanced neuro-interventions.
Risk of device-associated complications and side effects
Potential risks such as infections, lead migration, hardware malfunction, and stimulation-related side effects remain concerns that threaten the market's expansion. These complications may lead to device revision or explantation, increasing patient discomfort and treatment costs. Moreover, apprehensions about surgical implantation, long-term dependence, and possible interference with other bodily systems can deter both patients and physicians. Negative outcomes or high-profile product recalls could also impact public confidence in neuromodulation technologies.
The COVID-19 pandemic initially disrupted elective neuromodulation procedures due to lockdowns and resource reallocation toward critical care. Many patients delayed surgeries, leading to short-term declines in sales and implant volumes. However, post-pandemic recovery has been fueled by a renewed focus on chronic condition management and growing demand for outpatient-based treatments. Telehealth and remote device programming solutions also emerged as valuable tools, ensuring continuity of care and reshaping service delivery models in the neuromodulation sector.
The spinal cord stimulators segment is expected to be the largest during the forecast period
The spinal cord stimulators segment is expected to account for the largest market share during the forecast period propelled by the high prevalence of chronic back and leg pain disorders. These devices are widely used in treating failed back surgery syndrome and complex regional pain syndrome, with proven long-term efficacy. Continuous product innovations, such as closed-loop systems and wireless programming, enhance treatment outcomes and patient compliance. Moreover, favorable reimbursement policies in key markets further support the large-scale adoption of spinal cord stimulators.
The deep brain stimulators segment is expected to have the highest CAGR during the forecast period
Over the forecast period, the deep brain stimulators segment is predicted to witness the highest growth rate, influenced by increasing demand for advanced therapies in managing Parkinson's disease, dystonia, and essential tremor. Technological advancements in targeting precision and programming flexibility are improving patient outcomes. Furthermore, growing research in psychiatric and neuropsychiatric applications, including depression and OCD, is expanding the scope of deep brain stimulation. As clinical indications widen, the segment is positioned for accelerated global growth.
During the forecast period, the Asia Pacific region is expected to hold the largest market share, fuelled by, rising neurological disorder prevalence, growing healthcare expenditure, and increasing adoption of advanced medical technologies. Countries like China, Japan, and India are investing heavily in neurology infrastructure and device-based therapies. Moreover, growing patient awareness, expanding private healthcare networks, and supportive government initiatives in neurorehabilitation drive regional demand. The large population base and ongoing urbanization further strengthen Asia Pacific's dominance in the neuromodulation devices market.
Over the forecast period, the North America region is anticipated to exhibit the highest CAGR, driven by, rising neurological disorder prevalence, growing healthcare expenditure, and increasing adoption of advanced medical technologies. Countries like China, Japan, and India are investing heavily in neurology infrastructure and device-based therapies. Moreover, growing patient awareness, expanding private healthcare networks, and supportive government initiatives in neurorehabilitation drive regional demand. The large population base and ongoing urbanization further strengthen Asia Pacific's dominance in the neuromodulation devices market.
Key players in the market
Some of the key players in Neuromodulation Devices Market include Medtronic, Boston Scientific Corporation, Stryker, Abbott, B. Braun Melsungen AG, NEVRO CORP., NeuroSigma, Inc, NeuroPace, Inc., Soterix Medical Inc, Synapse Biomedical Inc, ReShape Lifesciences, Inc, Bioness Inc., ALEVA NEUROTHERAPEUTICS SA, LivaNova PLC, Neuronetics, Cyberonics, Inc., Neuromod, and Axonics, Inc.
In July 2025, Boston Scientific received FDA approval for two new SCS leads-Linear 3-4 and Linear 3-6-for its Precision Plus SCS System, expanding percutaneous lead configuration options in the market.
In April 2025, Abbott introduced a next-generation delivery system for its Proclaim(TM) DRG neurostimulation-the first FDA-approved DRG technology for treating complex regional pain syndrome (CRPS) types 1 & 2-designed to streamline electrode placement to the dorsal root ganglion.
In January 2025, Medtronic achieved CE mark approval for its BrainSense Adaptive Deep Brain Stimulation (aDBS) and Electrode Identifier systems-a significant milestone enabling personalized, sensing-enabled care for Parkinson's patients in Europe.
Note: Tables for North America, Europe, APAC, South America, and Middle East & Africa Regions are also represented in the same manner as above.