CORD, LLC, a privately held ophthalmic medical device company, today announced results from its one-year follow-up on patients who were implanted with the Model SC9 intraocular lens (IOL) in a clinical trial.
ALISO VIEJO, Calif., Nov. 11, 2021 /PRNewswire/ -- CORD, LLC, a privately held ophthalmic medical device company, today announced results from its one-year follow-up on patients who were implanted with the Model SC9 intraocular lens (IOL) in a clinical trial. The trial was performed under an Investigational Device Exemption (IDE) with the U.S. Food and Drug Administration (FDA) for the treatment of cataracts. This important milestone enables the company to file a Premarket Approval (PMA) application to secure FDA approval for the commercial distribution of the Model SC9 in the United States. Cataracts, a consequence of aging, are a clouding over of the lens of the eyes, causing blurry vision. A treatment for cataracts is the surgical implantation of an IOL. While this common, minimally invasive surgical procedure is extremely effective at restoring vision, it comes with limitations, such as the continued need for glasses to correct imperfect intermediate and near vision; glare or halos that compromise distance vision; loss of contrast sensitivity; or loss of binocular vision. ABOUT THE MODEL SC9 INTRAOCULAR LENS
“Dr. Cumming has done it again,” said John Hovanesian of Harvard Eye Associates in Laguna Hills, California. “As one of the leading pioneers of IOL development, with the Model SC9 he’s showing that he has even more to offer the field of ophthalmology. This new lens offers patients a range of vision with a perfectly focused image.” ABOUT CORD, LLC AND INVENTOR STUART CUMMING, MD Media Contact
SOURCE CORD, LLC |