Optovue

6 recalls Categories: Diagnostic Equipment, Implants & Prosthetics

FDA determined that a 510(k) is needed for the Vault Mapping software (also known as Lens Fitting).

Jul 27, 2017 Diagnostic Equipment Nationwide View Details →

FDA determined that a 510(k) is needed for the Vault Mapping software (also known as Lens Fitting).

Jul 27, 2017 Diagnostic Equipment Nationwide View Details →

FDA determined that a 510(k) is needed for the Vault Mapping software (also known as Lens Fitting).

Jul 27, 2017 Diagnostic Equipment Nationwide View Details →

A software anomaly was detected that affects Optovue iVue and iVue 500 with Normative Database that may display images of the same eye rather than right and left if user scrolls on the map.

Mar 16, 2016 Diagnostic Equipment Nationwide View Details →

Devices labeled for an intended use not included in the existing 510(k) or PMA. Specifically, "The Retina" poster provided with the systems, and the book "RETINAL OCT Analysis and Interpretation Method" by Bruno Lumbroso and Marco Rispoli which are not labeled within 51O(k) cleared product description.

Sep 7, 2012 Implants & Prosthetics Nationwide View Details →