Soul Mobility is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Soul Mobility - FDA 510(k) Cleared Devices
Recent clearances: Power-Flex (PFX1214)
1
Total
1
Cleared
0
Denied
Soul Mobility has 1 FDA 510(k) cleared medical devices. Based in Oconomowoc, US.
Latest FDA clearance: Nov 2024. Active since 2024. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Soul Mobility Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Spectramedex, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Soul Mobility
1 devices