Argus retinal prosthesis, also known as a bionic eye, is an electronic retinal implant manufactured by the American company Second Sight Medical Products. It is used as a visual prosthesis to …

Oct 1, 2016 · Two generations of devices, the Argus I and Argus II, have been developed by SSMP. Argus I is a first-generation epiretinal prosthesis approved for a phase I clinical trial by …

The Argus As I was a four-cylinder, water-cooled, aircraft engine produced in Germany by Argus Motoren from 1911 until about 1913. The engine saw widespread use in aircraft in pre-war …

Dec 2, 2019 · The Argus II device (Second Sight Medical Products) is the only FDA-approved epiretinal implant at this time. In 2002, Argus I, the first iteration of the device, which had 16 …

Apr 9, 2020 · Objective: The Argus I implant is a first-generation epiretinal prosthesis approved for an investigational clinical trial in the U.S. Its successor, the Argus II implant, has a higher …

On February 14, 2013, the US Food and Drug Administration (FDA) approved the Argus II Retinal Prosthesis System, the first implanted device to treat adults with advanced retinitis pigmentosa …

Artificial retina devices (e.g., the Argus II); Artificial iris devices (e.g., the CustomFlex Artificial Iris) for anterior segment reconstruction, and the treatment of aniridia, post-operative or traumatic …

Purpose : The Argus I (Second Sight Medical Products) retinal implant, containing an array of 16 electrodes, is the first-generation epiretinal prosthesis approved for investigational clinical trials …

Mar 16, 2015 · The Argus II epiretinal prosthesis (Second Sight Medical Products) is currently the only retinal prosthesis approved by the Food and Drug Administration and Health Canada. In …

Argus I was the first-generation prototype of an epiretinal implant manufactured by Second Sight Medical Products.