Orthopaedic Spine & Trauma Implants
Orthopaedic Spine & Trauma Implants
Advancing Orthopaedic Solutions.
Eta Vizili Medical is a specialised manufacturer of advanced spinal and trauma implant systems, dedicated to delivering precision-engineered orthopaedic solutions that meet the highest international standards of quality, safety and performance. With a comprehensive portfolio of FDA-cleared implant systems, our products are distributed through a trusted network of authorised partners across more than 20 countries worldwide.
About
A manufacturer of spinal and trauma implants.
Eta Vizili is a medical device manufacturer founded in 2013 and based in Ankara, Türkiye. We design and produce implant systems for spine and trauma surgery and supply them to hospitals through authorised distributors.
- Two product familiesSpine and trauma.
- Eight implant systemsEach supplied with its own comprehensive range of surgical instruments.
- FDA 510(k) cleared · ISO 13485Technical documentation maintained for every family.
Products
Spinal and trauma implant systems.
Eight systems in two families. Spine covers lumbar and cervical fixation. Trauma covers plates, screws, intramedullary nails and craniomaxillofacial plates.
Lumbar
Posterior lumbar fixation and interbody fusion: pedicle screws, rods, connectors and cages.
Cervical
Anterior and posterior cervical fixation, interbody cages, corpectomy and motion preservation.
3.5 System
Small fragment plating: anatomic locking plates from the clavicle to the pelvis.
4.5 System
Large fragment plating for the lower extremity: femur, tibia, fibula and calcaneus.
Screws
Trauma screws from Ø 1.5 to Ø 7.3 mm: cortical, cancellous, cannulated, Herbert and headless.
Nail
Intramedullary nails for the femur, humerus and tibia, and a flexible nail.
Mini Plate
Mini fragment plates in 1.5, 2.0, 2.5 and 2.7 mm, including fusion plates.
Craniomaxillofacial Plate System
Craniomaxillofacial plates at 0.6 mm, with an orbital plate and a burr hole cover.
Quality & regulatory
Manufactured under a controlled quality system.
FDA 510(k) cleared
We are an exporter of FDA 510(k) cleared devices. They are supplied to markets outside the United States and are not distributed within the U.S.A.
ISO 13485 certified
Design, production and post-market surveillance run under a quality management system certified to ISO 13485.
Traceability
Every part is marked and traceable to its material lot, its machine and its inspection record.
Manufacturing
From bar stock to packaged implant.
- Design & engineering
Design reviews and manufacturability analysis are completed before production begins.
- Precision machining
Implants are machined to the drawing, with in-process measurement of critical dimensions.
- Finishing & surface
Deburring, polishing, colour-coding anodising, passivation and electropolishing.
- Inspection
Dimensional and optical inspection against the drawing. Records are kept for the life of the lot.
- Cleanroom & packaging
Ultrasonic cleaning and packing in a controlled environment.
Where we are
Supplied through distributors in more than 20 countries.
Our systems reach hospitals through authorised distribution partners. Each partner is supported with technical documentation and product training.