Method Mobility is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Method Mobility - FDA 510(k) Cleared Devices
Recent clearances: AMP by Method Mobility, AMP Plus (or +) by Method Mobility
1
Total
1
Cleared
0
Denied
Method Mobility has 1 FDA 510(k) cleared medical devices. Based in Fresno, US.
Last cleared in 2023. Active since 2023. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Method Mobility 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 - Method Mobility
1 devices