Orthoxel Dac is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Orthoxel Dac - FDA 510(k) Cleared Devices
Recent clearances: Vertex Hip Fracture Nailing System
1
Total
1
Cleared
0
Denied
Orthoxel Dac has 1 FDA 510(k) cleared medical devices. Based in Cork, IE.
Latest FDA clearance: Apr 2024. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Orthoxel Dac Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Orthoxel Dac
1 devices