Myolyn, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Myolyn, LLC - FDA 510(k) Cleared Devices
Recent clearances: MyoCycle MC-2 (Home / Home + / Pro / Pro +)
2
Total
2
Cleared
0
Denied
Myolyn, LLC has 2 FDA 510(k) cleared medical devices. Based in Gainesville, US.
Last cleared in 2022. Active since 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Myolyn, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Myolyn, LLC
2 devices