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Regain leg or hand function and improve mobility after a stroke or diagnosis of Multiple Sclerosis
or other Central Nervous System Disorders. Our Certified Clinical Specialists can meet
with you to see if Bioness technology is right for you.

WATCH FIRST IMPRESSIONS OF THE L300 Go!

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.

 

Indications for Use:
The H200 Wireless System is an electrical stimulation device indicated for the following uses:

• Functional Electrical Stimulation (FES)
• Improvement of hand function and active range of motion in patients with hemiplegia due to stroke or upper limb paralysis due to C5 spinal cord injury.
• NeuroMuscular Electrical Stimulation (NMES)
• Maintenance and/or increase of hand range of motion; Prevention and/or retardation of disuse atrophy; Increase in local blood circulation; Reduction of muscle spasm; Re-education of muscles.

H200 Wireless is contraindicated in patients with a demand-type cardiac pacemaker, defibrillator or any electrical implant. Do not use the system on a hand where metallic implant is directly underneath the electrodes, a cancerous lesion is present or suspected, or on a hand 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/h200/safety-information/.

All revisions of the Instructions for Use / Patient Guides and Reference Cards can be made available upon request.
Contact bionessrehab@bioventus.com or 800-211-9136 to request an electronic copy.

H200^® Wireless, L300 Go^®, Bioness, the Bioness Logo^® are registered trademarks of Bioness Inc. | www.bionessrehab.com

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L300 Go^® System

The Bioness L300 Go uses Functional Electrical Stimulation (FES) technology to help you lift your foot to walk more naturally and safely.

H200^®  Wireless System

The H200 Wireless Hand Rehabilitation System uses Functional Electrical Stimulation (FES) technology to improve arm and hand motion.

LEARN ABOUT THE H200 WIRELESS SYSTEM!