Medical Device Manufacturer · US , Grand Junction , CO

Opti-Centre Laboratories - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1998

Recent clearances: PROCLEAR ULTRAVUE MULTIFOCAL AND PROCLEAR ULTRAVUE 2000T MULTIFOCAL TORIC (OMAFLICON A) SOFT (HYDROPHILIC CONTACT LENS), ULTRAVUE/P 2000T, ULTRAVUE/C 2000T (HIOXIFILCON B) SOFT (MULTIFOCAL TORIC) DAILY WEAR CONTACT LENS (CLEAR & BLUE VISIBIL, ULTRA VUE 55/P & C (METHAFILCON A) SOFT (MULTIFOCAL, SPHERICAL, & TORIC) DAILY WEAR CONTACT LENS (CLEAR & BLUE VISIBILIT

View 6 510(k) Devices ↓

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.

Opti-Centre Laboratories is one of 23000 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Opti-Centre Laboratories

6 devices

1-6 of 6

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