Why L100 Go

Technology You Can Trust

Comfortable, Easy-to-Use, Move Naturally

FES complements an AFO5
Research has demonstrated the ability of functional electrical stimulation to improve clinical outcomes.1-4

null
40%
improvement in walking speed3
null
30%
improvement in distance walked4

45+ Research Articles and Level 1A Evidence

Support the use of FES to improve gait, balance and independence.1,2

Walk More Naturally

3D Motion DetectionAdaptive algorithm to detect gait events, providing precise stimulation when needed.

Mobile Application The myBioness™ app allows patients to control their system, set goals and track activity.

Comfortable, Lightweight Leg Cuff The “patella locator” ensures consistent electrode placement, allowing easy set-up, and can be put on with one hand. On-board controls allow for simple management.

Contact us to schedule a demo with L100 Go or if you have questions about other Bioness products.

Contact Us
  1. O’Dell MW, Dunning K, et al. Response and prediction of improvement in gait speed from functional electrical stimulation in persons with poststroke drop foot. PM&R. 2014;6(7):587-601; quiz 601. doi:10.1016/j.pmrj.2014.01.001
  2. Teasell R, et al. Evidence-Based Review of Stroke Rehabilitation: Executive Summary, 18th Edition. Heart & Stroke Foundation. 2016; 1-66
  3. Bethoux F, Rogers HL, et al. The effects of peroneal nerve functional electrical stimulation versus ankle-foot orthosis in patients with chronic stroke: a randomized controlled trial. Neurorehabil Neural Repair. 2014:28(7):688-97. doi:10.1177/1545968314521007
  4. Hausdorff JM, Ring H. Effects of a New Radio Frequency– Controlled Neuroprosthesis on Gait Symmetry and Rhythmicity in Patients with Chronic Hemiparesis. Am J Phys Med Rehabil. 2008; 87(1): 4-13
  5. Kluding P, Dunning K, O’Dell M, et al. Foot Drop Stimulation vs Ankle Foot Orthosis Following Stroke: 30 week outcomes. Stroke. 2013. Jun;44(6):1660-9.

Indication for Use:The L100 Go System is indicated for use in adults with foot drop secondary to upper motor neuron pathology in patients otherwise ambulatory. The device electrically stimulates muscles in the affected leg to provide ankle dorsiflexion of the foot; thus, it also may improve gait

The L100 Go System 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 https://bionessmedical.com/l100/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.