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Degen 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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LinkedIn
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Facebook
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Email
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Phone
—
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 10 of 151
DeviceModel / ReferenceRegistriesClassStatus
F1 MPS Modular Pedicle Screw System 0107-55045
FDA UDI
Class IIActive
Impulse AM Interbody Spacer System 0722-0936L08
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1201-362613L15
FDA UDI
Class IIActive
Hyper-C Anterior Cervical Plate System 0210-4088T
FDA UDI
Class IIActive
E³ MIS Pedicle Screw System 0602-70035
FDA UDI
Class IIActive
Impulse AM Interbody Spacer System 0724-0926N
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1203-382613L15
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1211-5535
FDA UDI
Class IIActive
Impulse Interbody Spacer System 07-34T1332N
FDA UDI
Class IIActive
Impulse Interbody Spacer System 07-09D10
FDA UDI
Class IActive
F1 MPS Modular Pedicle Screw System 0102-70085
FDA UDI
Class IIActive
F1 MPS Modular Pedicle Screw System 0110-85095
FDA UDI
Class IIActive
E³ MIS Pedicle Screw System 06-38G95
FDA UDI
Class IActive
Impulse Interbody Spacer System 07-36T1332N
FDA UDI
Class IIActive
Impulse Interbody Spacer System 07-04T0722L08
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 0301-5518L
FDA UDI
Class IIActive
F1 MPS Modular Pedicle Screw System 0104-55500
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-74D10
FDA UDI
Class IActive
Impulse Interbody Spacer System 07-06T1322N
FDA UDI
Class IIActive
Hyper-C Anterior Cervical Plate System 0210-2025T
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1201-322416L25
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1201-342612L05
FDA UDI
Class IIActive
Impulse Interbody Spacer System 07-36T1026L12
FDA UDI
Class IIActive
Impulse Interbody Spacer System 07-04T1126L12
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-04T402615L05
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-04T342417L00
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1201-362613L10
FDA UDI
Class IIActive
Impulse Interbody Spacer System 07-02T1636L08
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 0303-1214A
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1201-402813L10
FDA UDI
Class IIActive
Impulse Interbody Spacer System 07-06T1032A
FDA UDI
Class IIActive
E³ MIS Pedicle Screw System 0602-55050
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 0301-0912P
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-11S3024
FDA UDI
Class IActive
Solar™ Interbody Fusion System 1201-422815L15
FDA UDI
Class IIActive
DeGen Standard Instrumentation 99-89M
FDA UDI
Class IActive
Latitude-C Cervical Interbody Spacer System 03-04T1318
FDA UDI
Class IIActive
Hyper-C Anterior Cervical Plate System 0202-4218F
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1203-342415L25
FDA UDI
Class IIActive
Impulse Interbody Spacer System 07-06T1626L12
FDA UDI
Class IIActive
Impulse AM Interbody Spacer System 0722-1322A
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 0303-1314P
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 0301-0716L
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-04T342613L20
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1203-342616L25
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1201-322411L00
FDA UDI
Class IIActive
Impulse Interbody Spacer System 07-34T1526L12
FDA UDI
Class IIActive
Impulse AM Interbody Spacer System 0722-1232L08
FDA UDI
Class IIActive
Impulse Interbody Spacer System 07-04T0932N
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1203-423021L15
FDA UDI
Class IIActive

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