What is the L300 Go?

The L300 Go uses functional electrical stimulation (FES) to help people with certain medical conditions walk more confidently and achieve greater independence.

The brain sends electrical signals through the nervous system to tell the body how to move. When injury or disease disrupts communication between the brain and the lower extremities, muscle weakness or paralysis may result.

Sometimes, a muscle and its nerve supply remain healthy but communication from the brain cannot occur due to a central nervous system problem. In these cases, the L300 Go can detect gait irregularities and then deploy low-level corrective nerve stimulation to produce movements or functions that mimic the user’s natural voluntary actions. This helps users lift their feet correctly when walking.

With continued stimulation over time, the brain may even recapture the movement and relearn how to perform it without FES.

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The L300 Go is intended for people coping with foot drop and thigh weakness caused by:

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Stroke

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Multiple Sclerosis

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Cerebral Palsy

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Traumatic Brain injury

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Incomplete Spinal Cord Injury

L300 Go Features

  • 3D motion detection triggers stimulation precisely when needed.
  • Multichannel stimulation allows for precise control.
  • Quick setup gets users on their feet and walking sooner.
  • Outcome measures make it easy to track and document progress.
  • The mobile app lets users set goals, monitor activity, and track progress.

L300 Go Configurations

How does the L300 Go work?

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Have questions about L300 Go? Check out common questions and concerns on the FAQs page.

Contact us to schedule a demo with L300 Go or if you have questions about other Bioness products.

Indications for Use: The L300 Go System is intended to provide ankle dorsiflexion in adult and pediatric individuals with foot drop and/or to assist knee flexion or extension in adult individuals with muscle weakness related to upper motor neuron disease/injury (e.g., stroke, damage to pathways to the spinal cord). The L300 Go System electrically stimulates muscles in the affected leg to provide ankle dorsiflexion of the foot and/or knee flexion or extension; thus, it also may improve the individual’s gait.

The L300 Go System may also facilitate muscle re-education, prevent/retard disuse atrophy, maintain or increase joint range of motion, and increase local blood flow.

L300 Go is contraindicated in patients with a demand-type cardiac pacemaker, defibrillator or any electrical implant. Do not use the system on a leg where metallic implant is directly underneath the electrodes, a cancerous lesion is present or suspected, or on a leg with regional disorder (e.g., fracture or dislocation) which could be adversely affected by motion from the stimulation. Use caution in patients with diagnosed or suspected cardiac problems or epilepsy.

Full prescribing information can be found in product labeling or at: www.bionessrehab.com/l300/safety-information.

Instructions for Use / Patient Guides and Reference Cards can be made available upon request.
Contact [email protected] 
or 800-211-9136 to request an electronic copy.