Max Mobility, LLC is one of 18986 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Max Mobility, LLC - FDA 510(k) Cleared Devices
Recent clearances: SmartDrive Wheelchair Power Assist, SMARTDRIVE WHEELCHAIR POWER-ASSIST, HIROLLER ELEVATING WHEELCHAIR
3
Total
3
Cleared
0
Denied
Max Mobility, LLC has 3 FDA 510(k) cleared medical devices. Based in Antioch, US.
Historical record: 3 cleared submissions from 2010 to 2015. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Max Mobility, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Max Mobility, LLC
3 devices