Eusa Pharma (Uk) Limited is one of 439 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Eusa Pharma (Uk) Limited - FDA 510(k) Cleared Devices
Recent clearances: Caphosol® Artifical Saliva (32 doses sachet box), Caphosol Artifical Saliva Tablets
2
Total
2
Cleared
0
Denied
Eusa Pharma (Uk) Limited has 2 FDA 510(k) cleared medical devices. Based in Hemel Hempstead, GB.
Latest FDA clearance: Mar 2024. Active since 2017. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Eusa Pharma (Uk) Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Delphi Consulting Group as regulatory consultant.
FDA 510(k) Regulatory Record - Eusa Pharma (Uk) Limited
2 devices