Medical Device Manufacturer · US , Gainesville , FL

Myolyn, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2017

Total

Cleared

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) cleared devices by Myolyn, LLC

2 devices

1-2 of 2