Opti-Centre Laboratories is one of 9846 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Opti-Centre Laboratories - FDA 510(k) Cleared Devices
Recent clearances: RESOLUTION 5X (SPHERICAL) AND ULTRA GEL 5X (TORIC)(HIOXIFILCON A) SOFT DAILY WEAR CONTACT LENS, (CLEAR & BLUE VISIBILITY, RESOLUTION 45 (SPHERICAL) AND ULTRA GEL (TORIC) (HIOXIFILCON B) SOFT DAILY WEAR CONTACT LENS, )CLEAR & BLUE VISIBILITY T, ULTRAVUE/P, ULTRALVUE/C (HIOXIFILCON B)) SOFT (MULTIFOCAL) DAILY WEAR CONTACT LENS (CLEAR & YINTED, LATHE-CUT FROM LENS)
6
Total
6
Cleared
0
Denied
Opti-Centre Laboratories has 6 FDA 510(k) cleared medical devices. Based in Grand Junction, US.
Historical record: 6 cleared submissions from 1998 to 2005. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Opti-Centre Laboratories Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Opti-Centre Laboratories
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