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Find your ideal treatment option

At Boston Scientific, we offer Deep Brain Stimulation (DBS) options designed to fit your lifestyle. Every system comes with our advanced technology and exceptional customer support. Partner with your care team to select the DBS System that best matches your needs.

A DBS system consists of two main components

The system includes surgically placed leads in the brain and a battery, also called an Implantable Pulse Generator (IPG), that powers the system. The battery is typically placed under the skin near the collarbone and connects to the leads via extension wires.

The leads

Vercise™ Cartesia™ X and Vercise™ Cartesia™ HX Directional Leads​

The first and only 16-contact directional leads. These leads offer the best in span, spacing and directionality.*​

Why this matters: The longer directional span and tight spacing allow for more precise targeting of your neural structures, maximizing effectiveness while avoiding unwanted side effects.

The battery

Boston Scientific offers the broadest portfolio of batteries on the market.**

Whether you choose non-rechargeable or rechargeable, both types of batteries are designed to be thin and lightweight with smooth, gently rounded edges. This not only improves comfort but also helps to conceal signs of the implant.​

Non-rechargeable

A maintenance-free option that requires surgical replacement when depleted.

Perfect for patients who prefer not to worry about regular charging.​

Rechargeable

A smaller, longer-lasting device designed for at-home recharging on a weekly or monthly schedule.

Ideal for patients who are comfortable maintaining a charging routine.

Programming the system

Having the most advanced hardware is only part of the solution. What truly sets Boston Scientific apart is our unique and innovative approach to programming. Our proprietary programming technology brings the full potential of these systems, ensuring you receive the most precise and effective therapy possible.

Discover Image Guided Programming (IGP)

How to charge your DBS system

If you have been implanted with a rechargeable device, you will need to recharge periodically. We make it easy to recharge your battery via a wireless charging system. Depending on your therapy settings, you will only need to recharge your battery once a week or once a month. When it is time to recharge your system simply place the lightweight, wireless charging collar over your shoulders and relax — you can do it in front of the TV or while reading a book. Your remote will indicate how much charge is left in your battery.1

Understanding battery replacement

Batteries do not last forever; they need to be replaced when they reach the end of their expected life cycle. Battery replacement isn’t complicated, but it requires an outpatient procedure. The leads in your brain remain intact; only the battery in your chest will be replaced.

Switch your DBS IPG to Boston Scientific

If you’re a DBS patient with a system from either Abbott or Medtronic and it’s time to replace your IPG (Implantable Pulse Generator that includes the battery), you may be able to switch to Boston Scientific IPG. Boston Scientific IPGs are compatible with many Abbott or Medtronic systems. IPG replacement is an outpatient procedure and only the IPG in your chest will be replaced – not the leads in your brain.

See what doctors are saying

Dr. Richard Bucholz, St. Louis University, talks about the importance of choosing the right battery.

The right time to think about DBS is before you need it 

Take this short quiz and learn more. ⟶

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References

1. Yu X. Steinke K, Mustakos R. Characterizing rechargeable IPG charge cycle time in DBS. Presented at: North American Neuromodulation Society (NANS 2013)

*Best is defined as the directional lead with the longest directional span and most directional levels Boston Scientific. (2024). Vercise™ Deep Brain Stimulation Systems Surgical Implant Manual. https://www.bostonscientific.com/content/dam/elabeling/nm/92328632-05B_DBS_Surgical_Implant_Manual_US_EN_s.pdf Medtronic. (2021). Medtronic Sensight™ Directional Lead Kit. https://www.medtronic.com/content/dam/emanuals/neuro/M982097A_a_013_view.pdf Abbott. (2021).  Lead and Extensions Kits for Deep Brain Stimulation Systems. Clinician’s Manual. https://manuals.eifu.abbott/en/detail-screen.html

**The broadest portfolio in the industry is defined as offering the only 32-channel IPG available and a selection of 5 IPG devices, compared to 3 devices each from Medtronic and Abbott (as of March 2025) Abbott’s Neuromodulation for Movement Disorder. https://www.neuromodulation.abbott/us/en/healthcare-professionals/movement-disorders.html Medtronic’s Deep Brain Stimulation Systems. https://www.medtronic.com/me-en/healthcare-professionals/products/neurological/deep-brain-stimulation-systems.html

MR Conditional symbol

The Vercise Genus™ DBS System, Vercise Genus Mixed System with Vercise™ M8 Adapter, Vercise Genus Mixed System with Vercise™ Adapter S8, Vercise Gevia™ DBS System, and Vercise™ DBS Lead-only system (before Stimulator is implanted) provide safe access to full-body MRI scans when used with specific components and the patient is exposed to the MRI environment under specific conditions defined in the supplemental manual ImageReady™ MRI Guidelines for Boston Scientific DBS Systems.

MR not safe symbol

The Adapter S8 (for Abbott devices) is currently MR Unsafe.

Indication for Use: The Boston Scientific Vercise™ PC, Vercise Gevia™, Vercise Genus™ Deep Brain Stimulation Systems are indicated for use in:
-Bilateral stimulation of the subthalamic nucleus (STN) as an adjunctive therapy in reducing some of the symptoms of moderate to advanced levodopa-responsive Parkinson’s disease (PD) that are not adequately controlled with medication.
-Bilateral stimulation of the internal globus pallidus (GPi) as an adjunctive therapy in reducing some of the symptoms of advanced levodopa-responsive Parkinson’s disease (PD) that are not adequately controlled with medication.
-Unilateral thalamic stimulation of the ventral intermediate nucleus (VIM) is indicated for the suppression of tremor in the upper extremity. The system is intended for use in patients who are diagnosed with essential tremor or parkinsonian tremor not adequately controlled by medications and where the tremor constitutes a significant functional disability. 
-Bilateral stimulation of the ventral intermediate nucleus (VIM) of the thalamus for the suppression of disabling upper extremity tremor in adult essential tremor patients whose tremor is not adequately controlled by medications and where the tremor constitutes a significant functional disability.

The Boston Scientific Vercise Deep Brain Stimulation System is indicated for use in:
-Bilateral stimulation of the subthalamic nucleus (STN) as an adjunctive therapy in reducing some of the symptoms of moderate to advanced levodopa-responsive Parkinson’s disease (PD) that are not adequately controlled with medication.

Contraindications: The Boston Scientific Deep Brain Stimulation (DBS) Systems are not recommended for patients who will be exposed to the following procedures: Diathermy as either a treatment for a medical condition or as part of a surgical procedure, Electroconvulsive Therapy (ECT) and Transcranial Magnetic Stimulation (TMS).  The safety of these therapies in patients implanted with the Boston Scientific DBS System has not been established.  Patients implanted with Boston Scientific DBS Systems without ImageReady™ MRI Technology should not be exposed to Magnetic Resonance Imaging (MRI). Patients implanted with the Vercise Gevia or Vercise Genus or Vercise Genus Mixed System with M8 Adapter or Vercise DBS Lead-Only System (before Stimulator is implanted) with ImageReady MRI Technology are Full Body MR Conditional only when exposed to the MRI environment under the specific conditions defined in ImageReady MRI Guidelines for Boston Scientific DBS Systems.  Boston Scientific DBS Systems are not recommended for patients who are unable to operate the system or are poor surgical candidates or who experience unsuccessful test stimulation.

Warnings: Unauthorized modification to the medical devices is prohibited.  You should not be exposed to high stimulation levels.  High level of stimulation may damage brain tissue.  Patients implanted with a Boston Scientific DBS System may be at risk for intracranial hemorrhages (bleeding in the brain) during DBS lead placement.  Strong electromagnetic fields, such as power generators, security screeners or theft detection systems, can potentially turn the stimulator off, or cause unpredictable changes in stimulation. The system should not be charged while sleeping.  If you notice new onset or worsening depression, changes in mood or behavior or impulse control, or have thoughts of suicide contact your physician or emergency services immediately.  Chemical burns may result if the Stimulator housing is ruptured or pierced.  The Boston Scientific DBS Systems may interfere with the operation of implanted stimulation devices, such as cardiac pacemakers, implanted cardioverter defibrillators, or medication delivery pumps. Patients should operate motorized vehicles or potentially dangerous machinery with caution.  It is unknown if the device may hurt an unborn baby. Your doctor may be able to provide additional information on the Boston Scientific DBS Systems.  For complete indications for use, contraindications, warnings, precautions, and side effects, see DBSandME.com or call 833-DBS-INFO or 833-327-4636.
Caution: U.S. Federal law restricts this device to sale by or on the order of a physician.