Contamac, Ltd. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Contamac, Ltd. has 18 FDA 510(k) cleared ophthalmic devices. Based in Littleton, US.
Last cleared in 2022. Active since 2002.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Contamac, Ltd.
18 devices
Cleared
Mar 17, 2022
Optimum Infinite (tisilfocon A) Daily Wear Contact Lenses
Ophthalmic
210d
Cleared
Nov 23, 2018
Hyper GP (tisilfocon A) Daily Wear Contact Lens
Ophthalmic
91d
Cleared
Oct 22, 2018
Nutrifill
Ophthalmic
130d
Cleared
Apr 25, 2018
OPTIMUM GP (roflufocon D, roflurocon E) Daily Wear Contact Lens, HEXA100...
Ophthalmic
48d
Cleared
Oct 24, 2017
ENFLU 18 (enflufocon A) Daily Wear Contact Lens
Ophthalmic
147d
Cleared
Aug 01, 2017
HEXA100 (hexafocon A) Daily Wear Contact Lenses
Ophthalmic
112d
Cleared
Aug 10, 2016
Optimum GP with HPT (roflufocon A, B, C, D, and E) Daily Wear Contact Lenses
Ophthalmic
113d
Cleared
Jul 13, 2016
OPTIMUM GP OK Daily Wear Contact Lens (roflufocon D & E)
Ophthalmic
106d
Cleared
Jul 10, 2015
CONTAFLEX 54 (hioxifilcon D) Spherical Soft Contact Lens for Daily Wear,...
Ophthalmic
123d
Cleared
Oct 09, 2008
OPTIMUM HR-1.51 (HIFLUFOCON A) AND HR-1.53 (HIFLUFOCON B) DAILY WEAR CONTACT...
Ophthalmic
167d
Cleared
May 01, 2007
OPTIMUM GP (ROFLUFOCON A,B,C,D&E) DAILY WEAR CONTACT LENS.
Ophthalmic
55d
Cleared
Nov 01, 2006
MODIFICATION TO OPTIMUM GP (OXYGEN PERMEABLE) DAILY WEAR CONTACT LENSES
Ophthalmic
63d