Success Stories

Debra

In 2015, Debra suffered a hemorrhagic stroke that affected the left side of her body. She shares her story of the L300 Go helping her regain independence and finding hope to move forward.

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See how the L300 Go has changed other patients’ lives. Check out their success stories.

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

Indication 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 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.