Innova Vision, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Innova Vision, Inc. has 11 FDA 510(k) cleared ophthalmic devices. Based in Flagstaff, US.
Latest FDA clearance: Apr 2024. Active since 2004.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Eyereg Consulting, Inc. and Andre Vision and Device Research. 1 device has linked clinical trial registered on ClinicalTrials.gov.
11 devices
Cleared
Apr 17, 2024
Innova Vision (inifilcon A) Silicone Hydrogel (Hydrophilic) Daily Wear Soft...
Ophthalmic
54d
Cleared
CT
Nov 16, 2023
Innova Vision (inifilcon A) Silicone Hydrogel Soft (Hydrophilic) Contact Lens
Ophthalmic
121d
Cleared
Mar 13, 2023
Innova Vision Hydrogel (Etafilcon A) Soft (Hydrophilic) Contact Lens
Ophthalmic
167d
Cleared
May 13, 2022
Innova Vision Hydrogel (Hioxifilcon A) Soft (Hydrophilic) Contact Lens
Ophthalmic
228d
Cleared
Aug 17, 2012
CALAVIEW COLOR (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR...
Ophthalmic
366d
Cleared
Sep 03, 2009
DISCON PLUS (ETAFILCON A) CONTACT LENS VISIBILITY TINT WITH UV BLOCKER
Ophthalmic
300d
Cleared
Nov 29, 2007
CALAVIEW (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR
Ophthalmic
30d
Cleared
Jun 07, 2007
CALAVIEW COLORS (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS
Ophthalmic
281d
Cleared
May 12, 2006
DISCON DAILY (ETAFILCON A) ONE-DAY SOFT (HYDROPHILIC) CONTACT LENS
Ophthalmic
178d
Cleared
Aug 12, 2005
DISCON (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR
Ophthalmic
101d
Cleared
Mar 05, 2004
I-LUX INNOVA BLUE TINT LENS, MODEL SUPER O2
Ophthalmic
157d