Neuromodulation Market: Innovation Brings High-Growth Rewards

Neuromodulation is one of the largest and fastest growing segments of the worldwide medical device market, with global revenues expected to reach $6 billion by 2020;  as a result, the number of products in the neuromodulation pipeline is exploding. New and improved technologies will permit deeper penetration of neuromodulation therapies into existing patient groups as well as expansion of the market to new patient populations that could eventually number in the multi-millions.

Neuromodulation devices represent one of the largest and fastest growing segments of the worldwide medical device market. These technologies selectively alter or “modulate” the transmission of nerve impulses in the central, peripheral, or autonomic nervous systems or in the deep cell nuclei of the brain using programmable electrical or pharmacological therapies. Most of the neuromodulation devices sold today are implantable, and are used as a treatment of last resort to manage patients with chronic pain, movement disorders, spasticity, and epilepsy who do not respond to conventional therapies. But the number of products in the pipeline has exploded over the past five years as clinicians and manufacturers look to neuromodulation to treat an increasingly wide array of conditions and complex diseases, including chronic migraines, blindness, Alzheimer’s disease, depression, severe anorexia and other psychiatric disorders, epilepsy, obstructive sleep apnea, paralysis, asthma, blindness, stroke, heart failure, obesity, and incontinence. (See Exhibit 1.) Current and emerging neuromodulation devices include spinal cord stimulators, deep brain stimulators, cortical stimulators, peripheral nerve stimulators, neuroprosthetic devices, such as cochlear implants, and implantable drug delivery devices. (See Exhibit 2.) (See Also see "Device Start-Ups Inch Closer To Elusive Epilepsy Treatment" - Medtech Insight, 26 November, 2012., Also see "Deep Brain Provides Stimulating Market" - Medtech Insight, 25 April, 2012., and Also see "New Avenues in Neuromodulation" - Medtech Insight, 1 June, 2010..)

Exhibit 1

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Medtech Insight for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Asia

Industry Execs Talk Tariff Turbulence During MD&M East

 

During MD&M East in Manhattan last week, a panel of experts discussed how the Trump administration’s trade policy is affecting manufacturing and offered some ideas on what manufacturers can do to help mitigate the chaos.

India-UK Free Trade Agreement Sets Stage For Medtech Growth, But Industry Demands Safeguards

 
• By 

Announced after three years of negotiation, the FTA eliminates tariffs on 99% of Indian product types, covering nearly all trade value, and reduces tariffs on 90% of UK products. Although not yet formally signed, the deal is being positioned by the Indian government as “transformative,” with an estimated economic impact of $6.4bn for the UK alone by 2040.

Data Finds Capillary Blood Is A Reliable Alternative To Venous Blood For Routine Testing

 

A study from Babson Diagnostics published in the peer-reviewed Journal of Applied Laboratory Medicine showed that capillary blood sample volume issues can overcome historical challenges, such as poor quality, through a technique called assay miniaturization.

Medical Devices Not The Focus Of FDA’s Plans To Step Up Foreign Inspections, Expert Says

 

The US FDA recently announced plans to carry out more unannounced inspections of foreign facilities. But those inspections will primarily target drug producers, with less attention and resources allocated to those making devices.

More from Geography

Roche Diagnostics Day 2025: ‘We Need To Become A Leader In Decentralized Testing’

 

Roche aims to grow its diagnostics sales by mid to high single digits, said CEO of Roche Diagnostics Matt Sause. The company unveiled the Axelios synthesis and sequencing solution and discussed its “long-term commitment” to China, as well as its business strategy for the next five years.

Zika Virus Test Among 4 New FDA Device Classifications

 
• By 

The FDA plans to announce class II status for four new device types, including tests for the Zika virus and genetic condition Fragile X. This follows earlier announcements and highlights a trend toward diagnostic classifications. The classifications are considered deregulatory, meaning they will hel

FDA Draft Guidance Introduces Electric Submission For Q-Sub Process

 

The US FDA says its updated draft guidance represents one of several steps the agency is taking to develop electronic submission templates for the medical device industry. The document introduces stakeholders to currently available resources for supporting their pre-subs to the agency.