Degen Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Degen Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Solar™ Lumbar Interbody Fusion System, Cyclops™ Anterior Cervical Plate System
2
Total
2
Cleared
0
Denied
Degen Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Florence, US.
Latest FDA clearance: Jul 2024. Active since 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Degen Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Secure BioMed Evaluations as regulatory consultant.
FDA 510(k) Regulatory Record - Degen Medical, Inc.
2 devices