Ilker Kilinc's Colleagues at Zaraccom Lenses
Ilker Kilinc's Contact Details
Izmir,İzmir,Turkey
Zaraccom Lenses
Ilker Kilinc's Company Details
About Us;Zaraccom was founded in 2003 with the goal of developing the most scientifically advanced intraocular lenses (IOLs) and surgical products available for the ophthalmic industry.Zaraccom is the Turkey's first and largest intraocular lens manufacturer who has own unique Intraocular Lenses (IOLs) raw material and smart production methodology.Headquarter in Sivas, Turkey – in organized industrial zone – features an ISO 7 (Class 10,000), ISO 8 (Class 100,000), ISO 5 (Class 100) Clean rooms and state-of-the-art manufacturing process.Over 15 years we produced millions of Intraocular Lenses (IOLs) and sold out overall world: happy patients as millions.Zaraccom has a broad portfolio of products across the patient pathway, including monofocal and premium Intraocular Lenses (IOLs).Our R&D team always focus to improve product range and extra pure new Intraocular Lens (IOL) monomers for industry.Zaraccom is leading the way in ophthalmic innovation with Intraocular Lenses (IOLs) designed to provide surgeons and patients with the best visual outcomes.Quality;Zaraccom always works on maintaining and further strengthening the confidence of the market and the customers.Every members of the Zaraccom team identify themselves with the company's goals, are totally committed to these targets, and the realization of their individual and organizational pushes aimed at implementing them.The systems installed and operated at Zaraccom target the most efficient implementation of the company's mission. The efficiency of the system enables us to keep track of customers' feedback and the latest advances in science, as well as the prompt realization and implementation of the company's innovations based on this.Zaraccom 's quality management system fully complies with domestic and international laws, standards and regulations. Zaraccom continuously maintains compliance with the prevailing requirements of EN ISO 13485:2016, 93/42/EEC and for MDR transition process.