On December 15th 2006 we received the 510(k) premarket notification for our OCTAX LaserShot System (# K062524) by the Food and Drug Administration (FDA), Rockville MD, Department of Health & Human Services.
We are very pleased to announce that we successfully passed our DIN ISO 9001:2000 audit.
The introduction of a quality management system will strengthen our efforts to continuously provide our customers with high quality products and services