Eventum Orthopaedics, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Eventum Orthopaedics, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Quadsense (Quadsense and Quadsense Pro), QUADSENSE
2
Total
2
Cleared
0
Denied
Eventum Orthopaedics, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Leeds, GB.
Latest FDA clearance: Sep 2025. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Eventum Orthopaedics, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Eventum Orthopaedics, Ltd.
2 devices