
Get in touch
- 0090 2323 48 49 50 (pbx)
- info@prodorth.com
- RD Medikal Tıbbi Ürünler San. Tic. A.Ş Karacaoğlan Mah. Bornova Cad. No:9/G/1 Bornova IZMIR TURKEY 35070


Quality Management
Guided by our commitment to prioritize human well-being, we design and deliver innovative spinal solutions that enhance lives and foster trust in every partnership.


Our Quality
In our opinion, “A sustainable quality mentality” is the most critical fact for the permanency of a company. The main approach of PRODORTH is to maintain high quality products for the long run, an approach which aims at earning trust and building loyalty with our customers who we aim to serve for the long term.
Instead of using these certificates just as keys for trade, we prefer managing our business according the requirements of these systems. ISO 13485 Quality Management System is efficiently adapted on the organization of PRODORTH and provides a 100% traceability from initial to final product.
Our main task with respect to Quality Management is ensuring a complete control in a reliable and continuous production quality with machining, polishing, washing, color anodizing and laser marking units within our organization.
Biomechanical and biocompatibility tests were performed in accordance with ASTM and ISO standards which are required to launch our products to the market reliably, in addition all Prodorth products are firstly used by our surgeons and only launched to market after the succesful clinical outcomes are obtained.
PRODORTH has identified the problems during surgical operations and contacted surgeons on this issue. These feedbacks and internal discussions, analysis and wide researches provide new approaches which leads to new ideas.
Research and development to offer the innovative solutions will be always the priority of PRODORTH to which “R&D” initials were adopted.







































Our Certificates
All our manufacturing processes are followed up and managed in accordance with the medical device directive 93/42/EEC and a well-established ISO 13485 system. At the same time, the transition to the EU 2017/745 Medical Device Regulation (MDR) is in progress.









































