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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

Country
US
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Catalogue (485)

Page 8 of 10
DeviceModel / ReferenceRegistriesClassStatus
icotec Spine System, Screw Self-Tap, Ø 4.0 x 13 mm 12-70-40-133
FDA UDI
Class IIActive
KONG-TL VBR System, Implant Height Forceps 44-010
FDA UDI
Class IIActive
icotec Pedicle System 6.0, Rod, Ti, Curved, Ø 6.0 r120 x 090 mm 16-60-91209
FDA UDI
Class IIActive
icotec Ant. Cervical Plate, 1 Segmental, 21 mm 12-70-18-21
FDA UDI
Class IIActive
KONG-C VBR System, Screwdriver 43-030
FDA UDI
Class IIActive
VADERone Pedicle System, Screw, Carbon/PEEK, Polyaxial, Ø 5.5 x 30 mm 16-6023-55530
FDA UDI
Class IIActive
VADER Pedicle System, Rod, Ti, Curved, Ø 6.0 r120 x 80 mm 16-60-81208
FDA UDI
Class IIActive
icotec Lumbar Cage, Lumbar Cage ETurn TLIF, Container Lid 38-50-2
EUDAMEDFDA UDI
Class IIActive
icotec Lumbar Cage ETurn TLIF 08 x 16 mm 12-58-16-32-08-ITi
FDA UDI
Class IIActive
VADER Pedicle System Counter Torque Wrench 42-790
FDA UDI
Class IIActive
icotec Systems, Handle, 1/4" Coupling 42-892
FDA UDI
Class IIActive
icotec Ant. Cervical Plate, 4 Segmental, 86 mm 12-74-18-86
FDA UDI
Class IIActive
icotec Ant. Cervical Plate, 3 Segmental, 61 mm 12-73-18-61
FDA UDI
Class IIActive
KONG-TL VBR System, Trial Implant, S, Ø 19 mm x 28 mm 44-005-28
FDA UDI
Class IIActive
icotec Ant. Cervical Plate, 3 Segmental, 73 mm 12-73-18-73
FDA UDI
Class IIActive
icotec Lumbar Cage PLIF 8° / 25 mm x 11 mm 12-59-82511
FDA UDI
Class IIActive
icotec Cervical Cage Anatomic 8 x 18 mm 13-41-0818
FDA UDI
Class IIActive
icotec Lumbar Cage PLIF 0° / 25 mm x 15 mm 13-59-02515
FDA UDI
Class IIActive
VADER Pedicle System, Navigated Pedicle Probe, straight, for 6.5 mm Screw 42-530N
FDA UDI
Class IIActive
VADER Pedicle System, Navigated Cannulated Tap, Ø 7.5 mm 42-641N
FDA UDI
Class IIActive
VADER Pedicle System, Rod inserter, for cut rods 42-899
FDA UDI
Class IIActive
KONG-C VBR System, Trial End Plate, 0° / 14 x 13 mm 43-140
FDA UDI
Class IIActive
KONG-C VBR System, Trial Body, 20 mm 43-220
FDA UDI
Class IIActive
icotec Pedicle System 6.0, Rod, Ti, Straight, Ø 6.0 r000 x 200 mm 16-60-90020
FDA UDI
Class IIActive
icotec Ant. Cervical Plate, 3 Segmental, 76 mm 12-73-18-76
FDA UDI
Class IIActive
icotec Lumbar Cage PLIF 0° / 25 mm x 15 mm 12-59-02515
FDA UDI
Class IIActive
icotec Cervical Cage, Cervical Cage Anatomic, Container Base 41-12-1
FDA UDI
Class IIActive
LightMore Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Noncann., Ø 6.5 x 50 16-6024-56550
FDA UDI
Class IIActive
icotec Lumbar Cage ETurn TLIF 15 x 16 mm 13-58-16-32-15-ITi
FDA UDI
Class IIActive
icotec Lumbar Cage, Lumbar Cage PLIF, Container Inlay 1/2 38-60-3
EUDAMEDFDA UDI
Class IIActive
icotec Ant. Cervical Plate, 4 Segmental, 70 mm 12-74-18-70
FDA UDI
Class IIActive
KONG-C VBR System, KONG-C VBR M, Container, complete 43-090
FDA UDI
Class IIActive
KONG-C VBR System, Trial Body, 64 mm 43-264
FDA UDI
Class IIActive
icotec Pedicle System 6.0, Rod, Ti, Curved, Ø 6.0 r120 x 050 mm 16-60-91205
FDA UDI
Class IIActive
icotec Pedicle System 6.0, Rod, Ti, Curved, Ø 6.0 r120 x 040 mm 16-60-91204
FDA UDI
Class IIActive
VADER Pedicle System, Navigated Cannulated Tap, Ø 6.5 mm 42-631N
FDA UDI
Class IIActive
KONG-C VBR System, Trial Body, 40 mm 43-240
FDA UDI
Class IIActive
KONG-C VBR System, Trial Body, 42 mm 43-242
FDA UDI
Class IIActive
icotec Lumbar Cage PLIF 0° / 25 mm x 14 mm 13-59-02514
FDA UDI
Class IIActive
KONG-C VBR System, Height Forceps 43-040
FDA UDI
Class IIActive
KONG-C VBR System, KONG-C VBR M, Container Inlay 43-090-3
FDA UDI
Class IIActive
KONG-C VBR M, Body, 38 mm 12-80-1338-0
FDA UDI
Class IIActive
VADER Pedicle System, Dilator Navigated, Ø 13.0 mm 42-647N
FDA UDI
Class IIActive
KONG-TL VBR System, Torque Limiter with Coupling, 1/4'' Coupling, 1 Nm 44-074
FDA UDI
Class IIActive
icotec Lumbar Cage ETurn TLIF 13 x 12 mm 12-57-12-32-13-ITi
FDA UDI
Class IIActive
icotec Systems, Handle for deburrer, M6 42-894-1
FDA UDI
Class IIActive
KONG-TL VBR, End Plate, round, L and Screw, 8° x 43 mm 12-90-0843
FDA UDI
Class IIActive
VADER Pedicle System, Axial Connector, Ø 6.0 mm - Ø 6.0 mm 16-6060-0126
FDA UDI
Class IIActive
icotec Instrument, Rod Introducer 42-080
FDA UDI
Class IActive
KONG-C VBR M, Body, 26 mm 12-80-1326-0
FDA UDI
Class IIActive

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