Menicon Co, Ltd. is one of 23713 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Menicon Co, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Miru 1day UpSide (midafilcon A), MeniSept 3% Hydrogen Peroxide Cleaning & Disinfecting Solution, Miru 1day UpSide (midafilcon A)
19
Total
19
Cleared
0
Denied
Menicon Co, Ltd. has 19 FDA 510(k) cleared ophthalmic devices. Based in Washington, US.
Latest FDA clearance: Sep 2026. Active since 1994.
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 Foresight Regulatory Strategies, Inc., Andre Vision and Device Research and Foresight Regulatory Stategies, Inc..
FDA 510(k) Regulatory Record - Menicon Co, Ltd.
19 devices
Cleared
Sep 17, 2026
Miru 1day UpSide (midafilcon A)
Ophthalmic
59d
Cleared
Aug 13, 2026
MeniSept 3% Hydrogen Peroxide Cleaning & Disinfecting Solution
Ophthalmic
258d
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