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Icotec

US

Last updated May 24, 2026

Part of icotec AG

What Icotec makes

Icotec manufactures spinal fusion devices, including polymeric interbody cages for cervical and lumbar regions, non-bioabsorbable spinal screws and fixation plates, and reusable surgical tools such as bone taps, templates, and sterilization containers. Their portfolio also includes vertebral body replacement prostheses, spinal fixation rods (in titanium and carbon/PEEK composites), and specialized pedicle screw systems for internal stabilization.

The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. All products are designed for spinal surgical applications and comply with U.S. medical device standards.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Icotec manufacture?

Icotec specializes in spinal surgical devices, including polymeric spinal interbody fusion cages for cervical and lumbar regions, non-bioabsorbable spinal screws, fixation plates, and reusable surgical tools like bone taps and sterilization containers. Their portfolio also covers vertebral body prostheses, spinal fixation rods (made from titanium or carbon/PEEK composites), and advanced pedicle screw systems for internal spinal stabilization. These devices are designed to support spinal fusion, stabilization, and reconstruction procedures.

Where is Icotec based, and what regulatory region does it serve?

Icotec is based in the United States. While the company’s headquarters are in the U.S., its devices are developed and marketed in compliance with U.S. medical device regulations, including FDA requirements. This means their products are designed to meet the standards and regulatory expectations of the American healthcare system.

Which regulatory registries or databases list Icotec’s devices?

Icotec’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for spinal fusion and fixation products, allowing healthcare providers and regulators to identify and verify the devices in clinical and surgical settings. The UDI system is a key component of FDA compliance for medical devices in the U.S.

How are Icotec’s devices classified under FDA regulations?

All of Icotec’s devices fall under Class II classification according to FDA regulations. This classification applies to devices that generally pose moderate risk and require special controls to ensure their safety and effectiveness. Class II devices typically require premarket notification (510(k)) clearance unless they are exempt, demonstrating that they meet established regulatory standards for their intended use in spinal surgery.

What is the primary purpose of Icotec’s spinal fixation and fusion devices?

Icotec’s devices are primarily designed for spinal fusion and stabilization procedures. Their polymeric interbody cages promote bone growth between vertebrae, while non-bioabsorbable screws, plates, and rods provide structural support to maintain alignment during healing. Devices like vertebral body prostheses and pedicle screw systems address complex spinal deformities or injuries by restoring stability and facilitating long-term recovery. These products are engineered to address specific anatomical needs in cervical, lumbar, and thoracic regions.

AI-generated from registry data and not verified by a human reviewer.

Information

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US
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Catalogue (485)

Page 6 of 10
DeviceModel / ReferenceRegistriesClassStatus
icotec Cervical Cage Anatomic 8 x 18 mm 12-41-0818
FDA UDI
Class IIActive
LightMore Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Noncann., Ø 6.5 x 40 16-6024-56540
FDA UDI
Class IIActive
icotec Lumbar Cage ETurn TLIF 12 x 12 mm 13-57-12-32-12-ITi
FDA UDI
Class IIActive
icotec Lumbar Cage, Lumbar Cage ETurn TLIF, Container, complete 38-50
FDA UDI
Class IIActive
VADER Pedicle System, Trial rod, flexible, Ø 5.5 mm; L = 300 mm 42-895
FDA UDI
Class IIActive
LightMore Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Noncann., Ø 5.5 x 60 16-6024-55560
FDA UDI
Class IIActive
VADER Pedicle System VADER Pedicle System MIS 1/2 Container Base 42-853-1
FDA UDI
Class IIActive
KONG-C VBR System, Trial End Plate, 6° / 14 x 13 mm 43-146
FDA UDI
Class IIActive
KONG-TL VBR System, KONG-TL VBR E, Container Lid 44-090-2
FDA UDI
Class IIActive
KONG-C VBR, End Plate & Screw, 3° / 14 x 13 mm 12-80-301413
FDA UDI
Class IIActive
KONG-TL VBR System, KONG-TL VBR E, Container, complete 44-080
FDA UDI
Class IIActive
KONG-C VBR M, Body, 58 mm 12-80-1358-0
FDA UDI
Class IIActive
icotec Ant. Cervical Plate, 2 Segmental, 43 mm 12-70-18-43
FDA UDI
Class IIActive
KONG-TL VBR, End Plate, round, M and Screw, 12° x 33 mm 12-90-1233
FDA UDI
Class IIActive
KONG-TL VBR System, Trial Implant Holder 44-005-01
FDA UDI
Class IIActive
KONG-TL VBR, End Plate, rectangular, XL and Screw, 8° x 52 mm 12-90-085220
FDA UDI
Class IIActive
icotec Pedicle System 6.0, Rod, Ti, Straight, Ø 6.0 r000 x 040 mm 16-60-90004
FDA UDI
Class IIActive
VADERone Pedicle System, Screw, Carbon/PEEK, Polyaxial, Ø 5.5 x 40 mm 16-6023-55540
FDA UDI
Class IIActive
icotec Cervical Cage, Lordotic, 8 mm x 16 mm 12-40-0816
FDA UDI
Class IIActive
VADER Pedicle System, Rod, Ti, Curved, Ø 6.0 r120 x 50 mm 16-60-81205
FDA UDI
Class IIActive
icotec Ant. Cervical Plate, 1 Segmental, 23 mm 12-70-18-23
FDA UDI
Class IIActive
VADER Pedicle System, K-wire Dispenser, Extra Long, Ø 1.6 x 600 mm, Ø 1.1 x 600 42-881
FDA UDI
Class IIActive
VADERone Pedicle System, Screw, Carbon/PEEK, Polyaxial, Ø 5.5 x 35 mm 16-6023-55535
FDA UDI
Class IIActive
KONG-TL VBR System, Trial Implant, L, Ø 19 mm x 35 mm 44-005-35
FDA UDI
Class IIActive
LightMore Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Noncann., Ø 5.5 x 50 16-6024-55550
FDA UDI
Class IIActive
KONG-TL VBR, End Plate, round, S and Screw, 12° x 26 mm 12-90-1226
FDA UDI
Class IIActive
VADER Pedicle System VADER Pedicle System 2/2 Container Lid 42-861-2
FDA UDI
Class IIActive
KONG-C VBR System, Trial Body, 18 mm 43-218
FDA UDI
Class IIActive
VADER Pedicle System, VADER Pedicle System Navigated Instruments, Container Lid 42-700-2
FDA UDI
Class IIActive
VADER Pedicle System, Cannulated Tap MIS, Ø 6.5 mm 42-632
FDA UDI
Class IIActive
KONG-C VBR M, Body, 56 mm 12-80-1356-0
FDA UDI
Class IIActive
icotec Lumbar Cage PLIF 4° / 25 mm x 15 mm 13-59-42515
FDA UDI
Class IIActive
icotec Cervical Cage, Lordotic, 7 mm x 16 mm 12-40-0716
FDA UDI
Class IIActive
VADER Pedicle System, Template for HT S-rods 42-896-1
FDA UDI
Class IIActive
KONG-TL VBR, Screw, M8 x 6.0 mm 12-90-00806
FDA UDI
Class IIActive
icotec Ant. Cervical Plate, 4 Segmental, 78 mm 12-74-18-78
FDA UDI
Class IIActive
LightMore Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Noncann., Ø 5.5 x 35 16-6024-55535
FDA UDI
Class IIActive
LightMore Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Noncann., Ø 7.5 x 30 16-6024-57530
FDA UDI
Class IIActive
icotec Lumbar Cage ETurn TLIF 9 x 12 mm 13-57-12-32-09-ITi
FDA UDI
Class IIActive
KONG-TL VBR, End Plate, rectangular, L and Screw, 4° x 43 mm 12-90-044320
FDA UDI
Class IIActive
icotec Lumbar Cage, Lumbar Cage PLIF, Container Inlay 2/2 38-60-4
FDA UDI
Class IIActive
icotec Pedicle System 6.0, Rod, Ti, Curved, Ø 6.0 r120 x 080 mm 16-60-91208
FDA UDI
Class IIActive
VADER Pedicle System, Hexagon screw driver 42-898
FDA UDI
Class IIActive
KONG-TL VBR System, Expansion Handle 44-040-01
FDA UDI
Class IIActive
KONG-TL VBR E, Expandable Body, S, Ø 19 mm x 20 - 24 mm 12-90-1920-9
FDA UDI
Class IIActive
icotec Ant. Cervical Plate, 3 Segmental, 67 mm 12-73-18-67
FDA UDI
Class IIActive
VADER Pedicle System K-wire Dispenser, long For K-wire 1.6 x 472 mm 42-880
FDA UDI
Class IIActive
KONG-TL VBR System, Trial Implant, XL, Ø 19 mm x 41 mm 44-005-41
FDA UDI
Class IIActive
icotec Lumbar Cage PLIF 4° / 25 mm x 10 mm 13-59-42510
FDA UDI
Class IIActive
KONG-TL VBR System, Trial Implant, L + ES, Ø 19 mm x 54 mm 44-005-54
FDA UDI
Class IIActive

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