June 1, 2016 (Baltimore, MD) Noxilizer, Inc., the company advancing the NO₂-based sterilization process for pharmaceutical, biotech and medical device manufacturers, is pleased to announce a 510(k) clearance from the US Food and Drug Administration (FDA) for a medical device terminally sterilized using Noxilizer’s nitrogen dioxide sterilization process. For the article, please look at the following. http://www.noxilizer.com/about-news-events.php#news_20160601