TECLens, a medical device manufacturer and SERVImed Industrial Spa, an ophthalmic medical devices manufacturer and distributor today announced their partnership aimed at development and FDA approval of a new combination product to treat keratoconus.
STAMFORD, Conn., Oct. 7, 2019 /PRNewswire/ -- TECLens, a medical device manufacturer and SERVImed Industrial Spa, an ophthalmic medical devices manufacturer and distributor today announced their partnership aimed at development and FDA approval of a new combination product to treat keratoconus. The new product under development will combine TECLens’ CXLens® ‘on-eye’ cross-linking system for corneal remodeling with SERVImed’s trans-epithelial RIBOCROSS riboflavin drug formulation. TECLens and SERVImed will pursue FDA approval for the combination product of CXLens® / RIBOCROSS to treat keratoconus that affects more than a million people in the US. Like Avedro, SERVImed’s RIBOCROSS holds an FDA orphan drug designation for its proprietary riboflavin formulation for the treatment of keratoconus in patients undergoing cornea cross-linking procedures. “The combination of SERVImed’s proven RIBOCROSS and TECLens’ proven CXLens® will provide patients with a comfortable, non-invasive alternative to the treatment of ectatic disorders. Unlike any other cross-linking system, CXLens® can treat both eyes simultaneously. Our combination product with RIBOCROSS will significantly increase clinical efficiency and procedure margin for physicians practicing corneal crosslinking,” said TECLens CEO, David Acker. “We are very excited about this partnership, and strongly convinced that the combination of TECLens’ technology and SERVImed’s expertise will provide patients and physicians with an innovative, more efficient and safer corneal cross-linking procedure, said SERVImed CEO, Francesco Napolitano. About TECLens (www.TECLens.com) About SERVImed Industrial Spa View original content to download multimedia:http://www.prnewswire.com/news-releases/teclens-and-servimed-industrial-spa-announce-a-partnership-to-pursue-us-fda-approval-for-trans-epithelial-corneal-cross-linking-300933118.html SOURCE TECLens |