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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
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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 9 of 151
DeviceModel / ReferenceRegistriesClassStatus
Latitude-C Cervical Interbody Spacer System 0304-0612A
FDA UDI
Class IIActive
E³ MIS Pedicle Screw System 0603-65095
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1202-322417L25
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-04T382820L25
FDA UDI
Class IIActive
F1 MPS Modular Pedicle Screw System 0110-60040
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 0304-1420A
FDA UDI
Class IIActive
Impulse AM Interbody Spacer System 0724-0822L08
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1201-402815L10
FDA UDI
Class IIActive
DeGen Standard Instrumentation 97-63G55
FDA UDI
Class IActive
E³ MIS Pedicle Screw System 0602-90115
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 0301-0516L
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 0302-1314P
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-04T382619L20
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1203-362416L00
FDA UDI
Class IIActive
Impulse Interbody Spacer System 07-34T1532A
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-04T362416L00
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-60M04
FDA UDI
Class IActive
Solar™ Interbody Fusion System 1201-342614L00
FDA UDI
Class IIActive
Impulse AM Interbody Spacer System 0724-1622L08
FDA UDI
Class IIActive
Impulse Interbody Spacer System 07-04T1122L08
FDA UDI
Class IIActive
E³ MIS Pedicle Screw System 06-39G70
FDA UDI
Class IActive
Cyclops Anterior Cervical Plate System 02-74G0516
FDA UDI
Class IActive
Latitude-C Cervical Interbody Spacer System 03-06T6514
FDA UDI
Class IIActive
E³ MIS Pedicle Screw System 0602-65085
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1201-362412L10
FDA UDI
Class IIActive
E³ MIS Pedicle Screw System 0602-90050
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 0301-1316P
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1211-5028
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-33N19
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-04T342415L20
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-04T402617L25
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1201-382611L05
FDA UDI
Class IIActive
F1 MPS Modular Pedicle Screw System 0107-55080
FDA UDI
Class IIActive
E³ MIS Pedicle Screw System 0603-90050
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-04T322412L10
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-04T342415L00
FDA UDI
Class IIActive
Impulse AM Interbody Spacer System 0722-1136A
FDA UDI
Class IIActive
Impulse Interbody Spacer System 07-36T1322L08
FDA UDI
Class IIActive
E³ MIS Pedicle Screw System 0602-70085
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 0301-1218P
FDA UDI
Class IIActive
F1 MPS Modular Pedicle Screw System 0114-80085
FDA UDI
Class IIActive
F1 MPS Modular Pedicle Screw System 0117-85050
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-04T362610L00
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1203-362417L30
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-04T382621L05
FDA UDI
Class IIActive
DeGen Standard Instrumentation 97-0004S0
FDA UDI
Class IActive
Impulse Interbody Spacer System 07-06T1332L08
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1201-342411L15
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 0301-0816L
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1201-402816L15
FDA UDI
Class IIActive

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