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The U.S. Food and Drug Administration (FDA) granted market approval to an artificial retina technology today, the first bionic eye to be approved for patients in the United States. The prosthetic technology was developed in part with support from the National Science Foundation (NSF). The device, called the Argus® II Retinal Prosthesis System, transmits images from a small, eye-glass-mounted camera wirelessly to a microelectrode array implanted on a patient's damaged retina. The array sends electrical signals via the optic nerve, and the brain interprets a visual image. While the Argus II is a major breakthrough in retinal prosthetics, researchers are continuing their research. This third-generation retina chip, itself still very early in the development stage, contains 1,000 electrodes and was developed by Wentai Liu, a professor of bioengineering at the UCLA Henry Samueli School of Engineering and Applied Science and his colleagues. Early engineering done by Liu and his team was licensed to Second Sight
for the Argus II Retinal Prosthesis System. The FDA approval currently applies to individuals who have lost sight as a result of severe to profoundretinitis pigmentosa (RP), an ailment that affects one in every 4,000 Americans. The implant allows some individuals...
