Our mission was to produce low-price/high-quality reprocessed products to reduce the cost of healthcare delivery while lessening the impact of surgical waste on our environment. By 2006, we had started construction on a high-tech facility for reprocessing single-use devices. During construction, we researched FDA guidelines and formulated a plan for global distribution.
In September of 07, we received our first 510K approval from the FDA. Since then, we have developed a select line of reprocessed Class I devices and endoscopic trocars. Though we are thoughtfully expanding our capabilities and product offerings, we will always emphasize quality over quantity.