E.A.M Benelux B.V is one of 139 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
E.A.M Benelux B.V - FDA 510(k) Cleared Devices
Recent clearances: QF10
1
Total
1
Cleared
0
Denied
E.A.M Benelux B.V has 1 FDA 510(k) cleared medical devices. Based in Almere, NL.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by E.A.M Benelux B.V Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Merona Regulatory Partners as regulatory consultant.
FDA 510(k) Regulatory Record - E.A.M Benelux B.V
1 devices