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# Bioness Mobile App for Electrical Stimulation Device Cleared
- URL: https://www.fdaweb.com/bioness-mobile-app-for-electrical-stimulation-device-cleared/
- Published: 2018-03-26T12:00:00.000Z
- Updated: 2026-09-14T23:55:11.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5141063

FDA has cleared a Bioness 510(k) for the myBioness mobile app for use with its L300 Go System, a functional electrical stimulation system that offers 3D motion detection of gait events and muscle activation using data from a three-axis gyroscope and accelerometer. Bionesss says the mobile app is intended to allow home users to control their L300 Go system, including the ability to change stimulation modes between gait and training along with adjusting personal pre-set intensities to meet their daily activity demands. It is designed, the company says, to keep users engaged in the rehabilitation process and motivated to meet their recovery goals while tracking activity, setting personal goals and reviewing progress over time.