CooperVision, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Clariti 1 day Multifocal (somofilcon A) Soft (Hydrophilic), Daily Disposable Contact Lens with UV Blocker, MyDay (stenfilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens, Avaira Vitality (fanfilcon A) Soft (Hydrophilic) Contact Lens, Avaira Vitality
97
Total
94
Cleared
0
Denied
FDA 510(k) Regulatory Record - CooperVision, Inc. Ophthalmic ✕
85 devices
Cleared
Jan 25, 2024
Clariti 1 day Multifocal (somofilcon A) Soft (Hydrophilic), Daily Disposable...
Ophthalmic
28d
Cleared
Feb 04, 2022
MyDay (stenfilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens, Avaira...
Ophthalmic
25d
Cleared
Oct 26, 2021
Avaira Vitality
Ophthalmic
28d
Cleared
Oct 20, 2020
Clariti 1 Day (somofilcon A), Clariti 1 Day Toric (somofilcon A), Clariti 1...
Ophthalmic
29d
Cleared
Mar 23, 2020
MyDay (Stenfilcon A) ASPHERE, MyDay (Stenfilcon A) TORIC, MyDay (Stenfilcon...
Ophthalmic
266d
Cleared
Apr 29, 2019
MyDay
Ophthalmic
17d
Cleared
Dec 11, 2018
Clariti 1 day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens...
Ophthalmic
146d
Cleared
Jul 13, 2016
Avaira Vitality (fanfilcon A) Soft (Hydrofilic) Contact Lens
Ophthalmic
112d
Cleared
Dec 23, 2013
AVAIRA SPHERIC AND TORIC (ENFILCON A) SOFT CONTACT LENS
Ophthalmic
27d
Cleared
Aug 30, 2013
SUS (STENFILCON A) CONTACT LENS
Ophthalmic
108d
Cleared
May 30, 2013
PROCLEAR (OMAFILCON A) SOFT HYDROPHILIC) CONTACT LENS
Ophthalmic
230d
Cleared
Apr 03, 2012
AVAIRA (ENFILCON A) CONTACT LENS
Ophthalmic
104d
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