Mobius Mobility is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mobius Mobility - FDA 510(k) Cleared Devices
Recent clearances: iBOT® PMD, iBOT Personal Mobility Device (iBOT PMD)
2
Total
2
Cleared
0
Denied
Mobius Mobility has 2 FDA 510(k) cleared medical devices. Based in Manchester, US.
Latest FDA clearance: Jan 2025. Active since 2021. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Mobius Mobility Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mobius Mobility
2 devices