Technology/Features

Through the use of functional electrical stimulation (FES), the L300 Go lets people with certain medical conditions walk more confidently and achieve greater independence.

The L300 Go is the world’s first FES system that integrates proprietary 3D motion detection. Through an adaptive, learning algorithm, the L300 Go detects gait events, providing stimulation precisely when needed making it easier for users to clear their foot at varying walking speeds, on stairs, ramps, and while navigating uneven terrain.”

L300 Go Features

See how the L300 Go works

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Learn about the importance of functional electrical stimulation (FES) and how L300 Go can improve the mobility of a patient.

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.

All revisions of the 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.