Neurology & Neurovascular

Top Trends per Segment in the U.S. Neurological Device Market

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Top Trends per Segment in the U.S. Neurological Device Market

Neuromodulation, neurovascular, and neurosurgical devices collectively make up iData’s U.S. neurological devices market report. Within the United States, the overall neurological device market is growing and our analysts expect it to continue the substantial growth pattern into 2026. The categories included within the U.S. neurological device market report include:  Cerebrospinal Fluid Management  Interventional Neuroradiology  Neuromodulation 

Emma MatrickTop Trends per Segment in the U.S. Neurological Device Market
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Medtronics Groundbreaking DTM™ Spinal Stimulation Used to Treat Chronic Pain

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Medtronics Groundbreaking DTM™ Spinal Stimulation Used to Treat Chronic Pain

Medtronic recently announced the three-month results from a large, multicenter randomized controlled trial (RT) showing statistically significant and superior back pain relief through Differential Target Multiplexed (DTM™) Spinal Cord Stimulation (SCS) compared to conventional SCS. Both therapies were evaluated using the Intellis™ neurostimulator. The trials began on the hypothesis of: Do glial and neuronal cells

iData ResearchMedtronics Groundbreaking DTM™ Spinal Stimulation Used to Treat Chronic Pain
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BioSerenity Announces FDA Clearance for Electroencephalography (EEG) Wearable Device System

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BioSerenity Announces FDA Clearance for Electroencephalography (EEG) Wearable Device System

BioSerenity, Inc., recently announced they received U.S. Food and Drug Administration (FDA) 510(k) clearance for the Neuronaute® Electroencephalography (EEG) System and IceCap® EEG wearable device that allows physicians to remotely monitor patients with epilepsy. In general, EEG devices record the electrical activity of neurons in the brain through electrodes placed on the scalp (non-invasive) or

iData ResearchBioSerenity Announces FDA Clearance for Electroencephalography (EEG) Wearable Device System
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LATEST!! Covid-19 Causes Major Impacts on Neurologic Disorders

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LATEST!! Covid-19 Causes Major Impacts on Neurologic Disorders

The novel coronavirus (COVID-19; SARS-CoV-2) pandemic has affected millions worldwide. There are still many unknowns surrounding this virus yet one thing is for sure, in serious cases the virus causes devastating effect on the body – and not just on the lungs. “Neurology Online Journal“ has published a new study showing that the COVID-19 virus

iData ResearchLATEST!! Covid-19 Causes Major Impacts on Neurologic Disorders
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NeuroPace RNS System Received FDA Approval for MRI Labeling

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NeuroPace RNS System Received FDA Approval for MRI Labeling

NeuroPace RNS System for Epilepsy Received FDA Approval for MRI LabelingNeuroPace announced that its RNS® System has received FDA approval for MRI labeling, increasing number treatment options for approximately one million patients living with drug resistant focal epilepsy. Similar to a pacemaker that responds to abnormal heart rhythms, the RNS® System is programmed to detect

iData ResearchNeuroPace RNS System Received FDA Approval for MRI Labeling
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Abbott’s Low Dose Neuromodulation Implant for Chronic Pain

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Abbott’s Low Dose Neuromodulation Implant for Chronic Pain

Abbott‘s Low-Dose Neuromodulation Implant for Chronic Pain, Proclaim XR, was recently featured at 2020 International CES. Proclaim XR can connect to Apple products via Bluetooth and to enables patients to have more control over their treatment to regulate their pain as needed. Treatment plans can be updated and modified as new therapies are approved and

iData ResearchAbbott’s Low Dose Neuromodulation Implant for Chronic Pain
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Medtronic Micro Neurostimulator Submitted to FDA

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Medtronic Micro Neurostimulator Submitted to FDA

Register to receive a free Global Neurological Devices Market Analysis, Size, and Trends Report synopsis and brochure. In a new submission to the FDA, Medtronic has presented its InterStim Micro neurostimulator and InterStim SureScan MRI leads into the neuromodulation device market for pre-market approval (PMA). The device is 80% smaller than what is currently in

iData ResearchMedtronic Micro Neurostimulator Submitted to FDA
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“Voltron” Imaging Tool Captures Brain Cell Action in Living Animals

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“Voltron” Imaging Tool Captures Brain Cell Action in Living Animals

Register to receive a free U.S. Market Report Suite for Neurological  Devices report synopsis and brochure While scientists have a variety of tools on hand to monitor and manipulate living brains, they still lack the ability to observe how large numbers of individual neurons operate in real time. Now, researchers at the Howard Hughes Medical Institute have

iData Research“Voltron” Imaging Tool Captures Brain Cell Action in Living Animals
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Stryker Launches Next-Gen Flow Diverter for Treatment of Brain Aneurysms

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Stryker Launches Next-Gen Flow Diverter for Treatment of Brain Aneurysms

Register to receive a free U.S. Market Report Suite for Neurological  Devices report synopsis and brochure Stryker recently launched the Surpass Evolve Flow Diverter following approval in March. Surpass Evolve is Stryker’s newest product release into the flow diversion space for the treatment of brain aneurysms. Improving on the already successful existing Surpass platform, this new device

iData ResearchStryker Launches Next-Gen Flow Diverter for Treatment of Brain Aneurysms
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Health Canada Approves NeuroCatch™ Brain Assessment System

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Health Canada Approves NeuroCatch™ Brain Assessment System

Register to receive a free U.S. Market Report Suite for Neuromodulation, Neurovascular, Neurosurgical and Monitoring Devices report synopsis and brochure NeuroCatch, Inc. has recently announced the approval of their NeuroCatch™ Platform for a medical device license as Canada’s first objective and rapid neuro-physiological brain function assessment system. The device assesses neurological function through the measurement of event-related

iData ResearchHealth Canada Approves NeuroCatch™ Brain Assessment System
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