Unilens Corp., USA is one of 21653 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Unilens Corp., USA - FDA 510(k) Cleared Devices
Recent clearances: CVue ADVANCED (hioxifilcon D) Soft (hydrophilic) Contact Lens, CVUE ADVANCED HYDRA VUE, SOF-FORM II, UNILENS, UNISITE, SIMULVUE, AQUAFLEX, LL-38, BAYVUE AQUAFLEX MTO, UNILENS 38, UNISOFT, SIMULVUE 38 LLBI 2,
14
Total
14
Cleared
0
Denied
Unilens Corp., USA has 14 FDA 510(k) cleared ophthalmic devices. Based in Largo, US.
Historical record: 14 cleared submissions from 1994 to 2014.
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) Regulatory Record - Unilens Corp., USA
14 devices
Cleared
Oct 30, 2014
CVue ADVANCED (hioxifilcon D) Soft (hydrophilic) Contact Lens
Ophthalmic
30d
Cleared
Oct 05, 2012
CVUE ADVANCED HYDRA VUE
Ophthalmic
122d
Cleared
Apr 20, 2011
SOF-FORM II, UNILENS, UNISITE, SIMULVUE, AQUAFLEX, LL-38, BAYVUE AQUAFLEX...
Ophthalmic
63d
Cleared
Oct 28, 2010
CVUE ADVANCED DEFINITIVE
Ophthalmic
253d
Cleared
Sep 11, 2008
CVUE ADVANCED (HIOXIFILCON D) SOFT (HYDROPHILIC) CONTACT LENS
Ophthalmic
23d
Cleared
Apr 13, 2005
AQUAFLEX 2 (TEFILCON) CONTACT LENS
Ophthalmic
23d
Cleared
Jul 07, 2004
C-VUE 55 TORIC (METHAFILCON A) MULTIFOCAL CONTACT LENS
Ophthalmic
22d
Cleared
Oct 17, 2000
AXION PLUS (METHAFILCON A) SOFT (HYDROPHILIC) ASPHERIC CONTRACT LENS
Ophthalmic
71d
Cleared
Apr 10, 1996
POWER PLUS (POLYMACON) SOFT (HYDROPHILIC) ASPHERIC CONTACT LENS
Ophthalmic
35d
Cleared
Mar 28, 1996
FREESOFT (POLYMACON) SOFT (HYDROPHILIC) ASPHERIC CONTACT LENS
Ophthalmic
62d
Cleared
Mar 28, 1996
SEESOFT (POLYMACON) SOFT (HYDROPHILIC) ASPHERIC CONTACT LENS
Ophthalmic
62d
Cleared
Jul 07, 1994
UNILENS 38 SOFT ASPHERIC CONTACT LENS
Ophthalmic
85d