ILUMARK received FDA 510(k)

March 8th

Feldkirchen, 8th March 2011 - ILUMARK received FDA 510(k) clearance on its  Navigation Markers. This approval confirms the safety of the ILUMARK Navigation Markers according to US laws and allows the distribution in the United States of America.

Holger Rossner, CEO of ILUMARK, was very pleased by this approval: “We are delighted about the approval of our Navigation Markers in the USA. The clearance confirms the quality of our Markers and of our quality system. It enables us to expand in the most important market for medical products. We are in the process of closing strategic distribution contracts with US distributors and look forward to serve new customers in the USA with our quality and service performance.”

After the successful introduction of ILUMARK Navigation Markers on the European market ILUMARK has now ideal conditions for international success.