Menicon Co, Ltd. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Menicon Co, Ltd. has 17 FDA 510(k) cleared ophthalmic devices. Based in Washington, US.
Historical record: 17 cleared submissions from 1994 to 2020.
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 Menicon Co, Ltd.
17 devices
Cleared
Jun 17, 2020
Miru 1day UpSide (midafilcon A)
Ophthalmic
194d
Cleared
Mar 02, 2020
Menicon 3% Hydrogen Peroxide Cleaning and Disinfecting Solution
Ophthalmic
234d
Cleared
May 16, 2018
One Day Flat Pack (hioxifilcon A) Daily Disposable Soft Contact Lens
Ophthalmic
48d
Cleared
Feb 22, 2018
Menicon ASRB (asmofilcon A) Silicone Hydrogel Soft Contact Lens
Ophthalmic
51d
Cleared
Nov 16, 2017
Menicon Progent Protein Remover for Rigid Gas Permeable Contact Lenses
Ophthalmic
48d
Cleared
Aug 28, 2015
Menicon Saline Rinse Solution
Ophthalmic
59d
Cleared
Jul 03, 2013
MENICON UNIQUE PH MULTI-PURPOSE SOLUTION
Ophthalmic
100d
Cleared
Jan 02, 2013
MENICON PROGENT PROTEIN REMOVER FOR RIGID GAS PERMEABLE CONTACT LENS
Ophthalmic
156d
Cleared
Apr 28, 2011
ONE DAY FLAT PACK
Ophthalmic
210d
Cleared
Feb 03, 2011
MENICON Z (TISILFOCON A) RIGID GAS PERMEABLE CONTACT LENS
Ophthalmic
59d
Cleared
Mar 09, 2010
MENICON PROGENT PROTEIN REMOVER FOR RIGID GAS PERMEABLE CONTACT LENSES
Ophthalmic
526d
Cleared
Sep 23, 2008
MENICON Z RIGID GAS PERMEABLE CONTACT LENS
Ophthalmic
124d