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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 4 of 151
DeviceModel / ReferenceRegistriesClassStatus
Solar™ Interbody Fusion System 1202-402817L20
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-04T342416L05
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1203-342419L15
FDA UDI
Class IIActive
Impulse AM Interbody Spacer System 0722-1122L08
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-04T402617L20
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1203-402812L10
FDA UDI
Class IIActive
F1 Mps 01-0002P0
FDA UDI
Class IActive
E³ MIS Pedicle Screw System 06-01S
FDA UDI
Class IActive
Impulse Interbody Spacer System 07-04T0832N
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 03-04T1118
FDA UDI
Class IIActive
E³ MIS Pedicle Screw System 0602-65060
FDA UDI
Class IIActive
Cyclops Anterior Cervical Plate System 0220-4100T
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 0302-0518L
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-04T402810L10
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1201-322417L20
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1202-362617L05
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1201-362420L10
FDA UDI
Class IIActive
Impulse Interbody Spacer System 07-36T1626L08
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1203-322412L15
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1201-342418L00
FDA UDI
Class IIActive
DeGen Standard Instrumentation 97-47P
FDA UDI
Class IActive
E³ MIS Pedicle Screw System 0603-75055
FDA UDI
Class IIActive
Hyper-C Anterior Cervical Plate System 0203-4517V
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 03-04T6520
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1203-423016L00
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1201-382815L20
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 03-06T7514
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-70D15
FDA UDI
Class IActive
Impulse Interbody Spacer System 07-36T1036N
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 0302-0812L
FDA UDI
Class IIActive
Impulse AM Interbody Spacer System 0722-1522A
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1203-402813L15
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 0302-1420L
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 0303-0816A
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 0304-0716A
FDA UDI
Class IIActive
DeGen Standard Instrumentation 97-53P
FDA UDI
Class IActive
DeGen Standard Instrumentation 99-82M
FDA UDI
Class IActive
Solar™ Interbody Fusion System 1211-5528
FDA UDI
Class IIActive
E³ MIS Pedicle Screw System 06-37H
FDA UDI
Class IActive
F1 MPS Modular Pedicle Screw System 0114-10050
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 0301-1118A
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 03-04T0816
FDA UDI
Class IIActive
Hyper-C Anterior Cervical Plate System 0210-2024T
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 12-04T362621L00
FDA UDI
Class IIActive
Impulse Interbody Spacer System 07-04T0832A
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1203-402609L10
FDA UDI
Class IIActive
Impulse Interbody Spacer System 07-06T1422A
FDA UDI
Class IIActive
Solar™ Interbody Fusion System 1203-423019L15
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 03-03T0818
FDA UDI
Class IIActive
Latitude-C Cervical Interbody Spacer System 03-06T1218
FDA UDI
Class IIActive

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