Eywa Srl is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Eywa Srl - FDA 510(k) Cleared Devices
Recent clearances: Limfa Therapy System (Limfa Therapy)
1
Total
1
Cleared
0
Denied
Eywa Srl has 1 FDA 510(k) cleared medical devices. Based in Rimini, IT.
Latest FDA clearance: May 2025. Active since 2025. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Eywa Srl Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Eywa Srl America as regulatory consultant.
FDA 510(k) Regulatory Record - Eywa Srl
1 devices