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Sign in to claim this brandDegen Medical
US
Last updated September 17, 2026
What Degen Medical makes
Degen Medical manufactures spinal implant devices including interbody fusion cages made of metallic, polymeric, and metal-polymer composite materials, as well as spinal bone screws, surgical screwdrivers, and bone levers/elevators. Their specific product lines include the Solar™ Interbody Fusion System, Latitude-C Cervical Interbody Spacer System, Impulse Interbody Spacer System, and F1 MPS Modular Pedicle Screw System.
The company's devices are regulated as Class I and Class II medical devices and are listed in the FDA Unique Device Identification (UDI) registry. Degen Medical is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What does Degen Medical manufacture?
Degen Medical manufactures spinal implant devices including interbody fusion cages made of metallic, polymeric, and metal-polymer composite materials, as well as spinal bone screws, surgical screwdrivers, and bone levers/elevators. Their specific product lines include the Solar™ Interbody Fusion System, Latitude-C Cervical Interbody Spacer System, Impulse Interbody Spacer System, and F1 MPS Modular Pedicle Screw System.
Where is Degen Medical based?
Degen Medical is based in the United States. The company operates within the US, developing and manufacturing spinal implant devices for medical use.
Which regulatory registries list Degen Medical's devices?
Degen Medical's devices are listed in the FDA Unique Device Identification (UDI) registry. This registry tracks medical devices through unique identifiers to ensure proper identification and tracking throughout their lifecycle.
How are Degen Medical's devices classified?
Degen Medical's devices are regulated as Class I and Class II medical devices. Class I devices pose the lowest risk and are subject to general controls, while Class II devices require additional controls such as special labeling requirements and performance standards to ensure safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 1321C N Cashua Dr, Florence, SC, 29501
- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
- 3010663372
- DUNS Number
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Catalogue (7501)
Page 3 of 151| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Latitude-C Cervical Interbody Spacer System | 0304-0514P | FDA UDI | Class II | Active |
| Latitude-C Cervical Interbody Spacer System | 0302-5516P | FDA UDI | Class II | Active |
| F1 Mps | 01-0009P0 | FDA UDI | Class I | Active |
| Impulse AM Interbody Spacer System | 0726-1532N | FDA UDI | Class II | Active |
| E³ MIS Pedicle Screw System | 0603-80080 | FDA UDI | Class II | Active |
| Latitude-C Cervical Interbody Spacer System | 0305-0816L | FDA UDI | Class II | Active |
| F1 MPS Modular Pedicle Screw System | 0114-80055 | FDA UDI | Class II | Active |
| Cyclops Anterior Cervical Plate System | 0221-4013V | FDA UDI | Class II | Active |
| Impulse Interbody Spacer System | 07-06T1126L08 | FDA UDI | Class II | Active |
| Latitude-C Cervical Interbody Spacer System | 03-02T1314 | FDA UDI | Class II | Active |
| E³ MIS Pedicle Screw System | 0603-50050 | FDA UDI | Class II | Active |
| E³ MIS Pedicle Screw System | 0603-80075 | FDA UDI | Class II | Active |
| Impulse Interbody Spacer System | 07-04T1422L12 | FDA UDI | Class II | Active |
| Solar™ Interbody Fusion System | 1202-402813L10 | FDA UDI | Class II | Active |
| Solar™ Interbody Fusion System | 1201-382616L25 | FDA UDI | Class II | Active |
| Solar™ Interbody Fusion System | 12-04T342416L15 | FDA UDI | Class II | Active |
| Solar™ Interbody Fusion System | 1203-342618L10 | FDA UDI | Class II | Active |
| Solar™ Interbody Fusion System | 1203-362419L10 | FDA UDI | Class II | Active |
| Solar™ Interbody Fusion System | 1203-342417L10 | FDA UDI | Class II | Active |
| Latitude-C Cervical Interbody Spacer System | 0304-0712A | FDA UDI | Class II | Active |
| Solar™ Interbody Fusion System | 1201-422816L05 | FDA UDI | Class II | Active |
| Impulse Interbody Spacer System | 07-04T1532L12 | FDA UDI | Class II | Active |
| Latitude-C Cervical Interbody Spacer System | 0302-0712A | FDA UDI | Class II | Active |
| Solar™ Interbody Fusion System | 1201-342613L15 | FDA UDI | Class II | Active |
| Solar™ Interbody Fusion System | 12-04T382815L15 | FDA UDI | Class II | Active |
| DeGen Standard Instrumentation | 97-02R12 | FDA UDI | Class I | Active |
| Impulse Interbody Spacer System | 07-34T1232N | FDA UDI | Class II | Active |
| Solar™ Interbody Fusion System | 1210-5030 | FDA UDI | Class II | Active |
| DeGen Navigated Instrumentation | 15-24PS | FDA UDI | Class II | Active |
| F1 Mps | 01-50M | FDA UDI | Class I | Active |
| Latitude-C Cervical Interbody Spacer System | 03-05T0518 | FDA UDI | Class II | Active |
| Impulse AM Interbody Spacer System | 0724-1026A | FDA UDI | Class II | Active |
| Hyper-C Anterior Cervical Plate System | 0201-4220F | FDA UDI | Class II | Active |
| Solar™ Interbody Fusion System | 1203-322419L20 | FDA UDI | Class II | Active |
| E³ MIS Pedicle Screw System | 06-18PT | FDA UDI | Class I | Active |
| F1 MPS Modular Pedicle Screw System | 0117-85070 | FDA UDI | Class II | Active |
| Latitude-C Cervical Interbody Spacer System | 0302-1012L | FDA UDI | Class II | Active |
| F1 MPS Modular Pedicle Screw System | 0116-55110 | FDA UDI | Class II | Active |
| F1 MPS Modular Pedicle Screw System | 0110-55060 | FDA UDI | Class II | Active |
| Cyclops Anterior Cervical Plate System | 0221-4014F | FDA UDI | Class II | Active |
| Latitude-C Cervical Interbody Spacer System | 0302-0820L | FDA UDI | Class II | Active |
| Impulse Interbody Spacer System | 07-02T1036N | FDA UDI | Class II | Active |
| Latitude-C Cervical Interbody Spacer System | 0303-1320P | FDA UDI | Class II | Active |
| Latitude-C Cervical Interbody Spacer System | 03-02T0916 | FDA UDI | Class II | Active |
| Latitude-C Cervical Interbody Spacer System | 0305-0916P | FDA UDI | Class II | Active |
| F1 MPS Modular Pedicle Screw System | 0117-80090 | FDA UDI | Class II | Active |
| F1 MPS Modular Pedicle Screw System | 0114-10030 | FDA UDI | Class II | Active |
| Solar™ Interbody Fusion System | 1201-402819L10 | FDA UDI | Class II | Active |
| Latitude-C Cervical Interbody Spacer System | 03-06T7520 | FDA UDI | Class II | Active |
| Solar™ Interbody Fusion System | 1203-342419L20 | FDA UDI | Class II | Active |
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