Degen Medical
Degen Medical holds FDA 510(k) medical device clearances, first cleared 2015, most recent 2025.
Top product codes for Degen Medical
Recent clearances by Degen Medical
- K251829 — DeGen Medical Patient Specific Implant (PSI) System
- K252737 — DeGen Medical Latitude-C AM Cervical Interbody Fusion System
- K250667 — DeGen Medical Patient Specific Implant (PSI) System
- K241077 — DeGen Medical Patient Specific Implant (PSI) System
- K231199 — Solar Lumbar Interbody Fusion System
- K223418 — DeGen Impulse AM System
- K213918 — DeGen Navigated Instrumentation
- K213901 — Cyclops Anterior Cervical Plate System
- K210090 — Impulse AM Interbody Fusion System
- K203816 — DeGen Navigated Instrumentation
- K201287 — Impulse Interbody Fusion System
- K173814 — DeGen Medical E3 MIS Pedicle Screw System
- K160926 — F1 MPS Modular Pedicle Screw System
- K151496 — Latitude-C Cervical Interbody Spacer System
- K150759 — Hyper-C Anterior Cervical Plate System
- K142531 — F1-Modular Pedicle Screw System
Data sourced from openFDA. This site is unofficial and independent of the FDA.