Mobius Mobility LLC

FDA Regulatory Profile

Summary

Total Recalls
1
510(k) Clearances
2
Inspections
2
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1965-2025Class IIiBOT PMD with software version 01.05.24. Personal Mobility Device.April 24, 2025

Recent 510(k) Clearances

K-NumberDeviceDate
K243442iBOT® PMDJanuary 30, 2025
K210920iBOT Personal Mobility Device (iBOT PMD)June 16, 2021