Healthcare Providers
L300 Go
Improved Mobility. Made Easier.TM
The L300 Go is a functional electrical stimulation (FES) system that can produce measurable mobility improvements in individuals with foot drop, knee instability, or thigh weakness caused by injury or upper motor neuron disease.
FES provides low-level stimulation that may replace the electrical signals from the brain and produce movements or functions that mimic natural voluntary actions. With continued stimulation over time, the brain may even recapture the movement and relearn how to perform it without FES.
The L300 Go detects gait irregularities and then deploys corrective FES to help patients lift their feet correctly when walking. The system is intended for people coping with paralysis or paresis caused by:
The L300 Go’s User Benefits:
Benefits Comparison
L300 Go vs. ankle and foot orthoses (AFO)
| Benefit | L300 Go | AFO |
|---|---|---|
| Neuroplasticity promotion | Yes | No |
| Carry-over effect when not wearing device | Yes | No |
| Improved range of motion | Yes | No |
| Improved critical balance measures | Yes | No |
| Muscle atrophy prevention | Yes | No |
| Superior patient satisfaction | Yes | No |
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.
