Alevio, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alevio, LLC - FDA 510(k) Cleared Devices
Recent clearances: SI-Cure Sacroiliac Joint Fusion System, SI-Cure Sacroiliac Joint Fusion System
2
Total
2
Cleared
0
Denied
Alevio, LLC has 2 FDA 510(k) cleared medical devices. Based in Birmingham, US.
Last cleared in 2023. Active since 2023. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Alevio, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Technologies as regulatory consultant.
FDA 510(k) Regulatory Record - Alevio, LLC
2 devices