Opti-Centre Laboratories - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Opti-Centre Laboratories Ophthalmic ✕
6 devices
Cleared
Jan 12, 2005
PROCLEAR ULTRAVUE MULTIFOCAL AND PROCLEAR ULTRAVUE 2000T MULTIFOCAL TORIC...
Ophthalmic
61d
Cleared
Mar 26, 2001
ULTRAVUE/P 2000T, ULTRAVUE/C 2000T (HIOXIFILCON B) SOFT (MULTIFOCAL TORIC)...
Ophthalmic
56d
Cleared
Jun 29, 2000
ULTRA VUE 55/P & C (METHAFILCON A) SOFT (MULTIFOCAL, SPHERICAL, & TORIC)...
Ophthalmic
73d
Cleared
Aug 26, 1999
RESOLUTION 5X (SPHERICAL) AND ULTRA GEL 5X (TORIC)(HIOXIFILCON A) SOFT DAILY...
Ophthalmic
24d
Cleared
Mar 29, 1999
RESOLUTION 45 (SPHERICAL) AND ULTRA GEL (TORIC) (HIOXIFILCON B) SOFT DAILY...
Ophthalmic
175d
Cleared
Mar 02, 1998
ULTRAVUE/P, ULTRALVUE/C (HIOXIFILCON B)) SOFT (MULTIFOCAL) DAILY WEAR CONTACT...
Ophthalmic
83d