The Vercise™ DBS controller

It's About Time you had control of your DBS therapy. Introducing a controller developed in partnership with patients and designed with you in mind.

Our DBS System Controller is now an app on smartphone.^* When you are implanted with a Boston Scientific DBS System, you’ll receive a smartphone that comes with our app already installed. You can control your therapy by using the same simple taps and swipes you're used to on a phone. This makes it easy to use while keeping your DBS System safe and connected.

Features

Vercise DBS controller display is easy to read.

Clear display

An easy-to-read screen shows your settings at a glance.

Vercise DBS controller display has large buttons for easier adjustment.

Larger buttons

Larger buttons allow for more comfortable interactions. Enjoy simple and precise adjustments.

Vercise DBS controller includes tutorials to help you navigate.

Step-by-step guidance

Built-in tutorials help you navigate features with confidence.

Vercise DBS controller provides update notices.

Future-ready technology

As your needs evolve, so does your remote. The remote has the capability to receive updates ensuring you always have access to the latest features.

Looking for support on your Vercise DBS Controller?

View a video guide that provides easy-to-follow instructions that walk you through every feature and function of the new Controller, ensuring you can operate it with confidence.

Frequently asked questions

We understand that transitioning to a new device can raise questions. Below, you'll find answers to the most common quesitons about our Controller app. If you don't find the answer you're looking for, our support team is always ready to help.

Access FAQ page

MRI mode instructions

Safety is our top priority when it comes to MRI procedures. The Vercise™ DBS Controller includes a dedicated MRI Mode that ensures your device operates safely during magnetic resonance imaging. These instructions will guide your clinician through activating MRI Mode, understanding the safety checks, and returning to normal operation after your scan.  

Before proceeding with any MRI procedure, always consult with your healthcare provider and ensure they are aware that you have an implanted device. They will provide specific guidance based on your individual situation and the type of MRI scan being performed.

Download MRI instructions

We’re here to help

If you need additional assistance or have questions not covered here, our support team is available through multiple channels.

(833) 327-1473

BSNDBSPatientCare@bsci.com

*The Vercise™ DBS Controller is compatible with the Vercise Genus™ Deep Brain Stimulation only. Please visit: https://www.bostonscientific.com/VerciseDBSController-compatibility for a list of compatible mobile devices.

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.

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.

NM-2199105-AA

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