Epimed International is one of 16075 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Epimed International - FDA 510(k) Cleared Devices
Recent clearances: Racz Neurostat RF Generator, RK EPIDURAL NEEDLE
2
Total
2
Cleared
0
Denied
Epimed International has 2 FDA 510(k) cleared medical devices. Based in Johnston, US.
Latest FDA clearance: May 2024. Active since 2008. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Epimed International Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Intertek Testing Services and Medical Device Academy.
FDA 510(k) Regulatory Record - Epimed International
2 devices