Devices

Device Recall Optovue iVue and iVue 500

Model / Serial
US and foreign (not yet provided) Software version 2016.0.0.127: Serial numbers: 21908, 26507, 26496, 26558, 22738, 26139, 26442, 25720, 25079, 25142, 23298, 21990, 23461, 24199, 25843, 26572, 26550, 22971, 26495, 22652, 26550, 22971, 26495, 22652, 25389, 23309, 23760, 21732-1, 23527, 20923, 21600, 21414, 20271, 23153, 22875, 23211. Software version 2016.1.0.127; Serial numbers forthcoming.
Product Classification
Ophthalmic Devices
Device Class
2
Implanted device?
No
Distribution
PA, CA, IL, HI. MO, CO, GA, ME, IN, AZ, WV, VA, FL, AR, UT, NE, IN, NV, LA, TN, KS, OK. Foreign distribution forthcoming
Product Description
iVue and iVue 500 (now called iScan) OCT systems with software version 2016.0.0.127 (USA only) and 2016.1.0.127 (out of US) || Opthalmic: iVue is a non-contact, high resolution tomographic imaging device. It is intended for in vivo imaging, axial cross-sectional and three-dimensional imaging and || measurement of anterior and posterior ocular structures, including retina, retinal nerve fiber layer, ganglion cell complex (GCC), optic disc, cornea, and anterior chamber the eye.
Manufacturer
Optovue, Inc.
1 Event
- Recall of Device Recall Optovue iVue and iVue 500

Manufacturer

Optovue, Inc.

Manufacturer Address
Optovue, Inc., 2800 Bayview Dr, Fremont CA 94538-6518
Manufacturer Parent Company (2017)
Optovue Inc.
Source
USFDA

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