I-See Vision Technology, Inc. is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
I-See Vision Technology, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
I-See Vision Technology, Inc. has 4 FDA 510(k) cleared medical devices. Based in Flagstaff, US.
Historical record: 4 cleared submissions from 2009 to 2015. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by I-See Vision Technology, Inc. Filter by specialty or product code using the sidebar.
I-See Vision Technology, Inc. — FDA 510(k) Products and Clearance History
4 devices
Cleared
Apr 15, 2015
EZvue UV, Soft Daily Wear Contact Lenses (ocufilcon D), EZvue Colors, Soft...
Ophthalmic
68d
Cleared
Jun 16, 2009
EZVUE (OCUFILCON D) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR
Ophthalmic
260d
Cleared
Jun 16, 2009
EZVUE (OCUFILCON D) 1-DAY SOFT (HYDROPHILIC)CONTACT LENS
Ophthalmic
260d
Cleared
Jun 16, 2009
EZVIEW (POLYMACON) SOFT (HYDROPHILLIC) CONTACT LENS FOR DAILY WEAR
Ophthalmic
260d