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As Tria Spine®, our primary priority is; to ensure the satisfaction of our doctors and the health of our patients by producing high quality products.

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ALIF Titanium Cage with Anchors & Screws

  • Titanium: (Ti6Al4V ELI) Alloy
  • Better stability
  • With anchors and screws
  • Safe
  • Advanced design
  • Anatomical shape
  • Biocompatibility
  • More fusion area
  • With back lock screw
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LorX® ALIF Titanium Cage is a posterior intracorporeal fusion device used for the correction and stabilization of the lumbar spine (L2 - S1) region for the treatment of lumbo-sacral spine diseases.

LorX® ALIF Titanium Cage is designed to be used two pieces in per level.

LorX® TLIF Titanium Cage is designed to be used with auxiliary spinal fixation systems (posterior screw-rod systems, anterior plate systems, anterior screw-rod systems, etc.) and is not recommended for use by itself.

The LorX® ALIF Titanium Cage is indicated at a maximum of two levels for patients who meet the indications and have adequate spinal strength.

KYRA® Correction Cord System uses a strong, flexible cable to apply pulls outside a scoliosis curve to straighten of the spine instead of metal rods. The system uses the growth process to permanently straighten the spine.

Fixation systems are indicated for skeletally immature patients who require surgical treatment to achieve and maintain the correction of progressive idiopathic scoliosis. It is not suitable for use by adults.


LorX ALIF Titanium Cage is indicated for the treatment of degenerative disc disease (DDD) with up to Grade 1 spondylolisthesis. DDD is defined as back pain of discogenic origin with the degeneration of the disc confirmed by historical and radiographic studies. The device system is designed in order to get to used easily with an autograft to facilitate additional fixation and fusion.


Contraindications include but are not limited to:

Any medical or surgical condition that prevents the potential benefits of spine surgery, pathological obesity, pregnancy, overwhelming osteoporosis, open wounds, extreme local inflammation, drug and / or alcohol addiction, mental illness, extreme old age, body sensitivity to implant material, and / or allergy that preclude the potential benefits of spine surgery , acute or chronic infections, lack of patient cooperation.

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Tria Spine® and products has international certificates of CE, ISO 9001, ISO 13485: 2016. In addition to international certificates including USA approval.

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Research & Development

Tria Spine® has 4 International Patents and 2 USA Patents.

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Tria Spine® headquarters in Ankara / Although found in Turkey; Tria Spine® operates in 24 countries all over the world.

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2021 - 9 New Product Range Planning to Launch 2022 and 2 New Product Range Planning to Launch

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