Medical Device Manufacturer · US , Grand Junction , CO

Westcon Contact Lens Co., Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1994

Total

Cleared

Denied

Westcon Contact Lens Co., Inc. has 9 FDA 510(k) cleared medical devices. Based in Grand Junction, US.

Historical record: 9 cleared submissions from 1994 to 2005. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Westcon Contact Lens Co., Inc. Filter by specialty or product code using the sidebar.

Westcon Contact Lens Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Westcon Contact Lens Co., Inc.

9 devices

1-9 of 9

Cleared Feb 01, 2005

HORIZON 59 OASIS (HIOXIFILCON A) DAILY WEAR CONTACT LENSES

K043540 · LPL

Ophthalmic · 41d

Cleared Feb 20, 2004

HORIZON (METHAFILCON A) DAILY WEAR SPHERE AND TORIC CONTACT LENSES

K031774 · LPL

Ophthalmic · 256d

Cleared Nov 26, 2002

HORIZON 38 (CLEAR) AND HORIZON 38 WESTINT (TINTED)

K023530 · LPL

Ophthalmic · 36d

Cleared Jun 29, 1999

W-55 (METHAFILCON A) CLEAR AND VISIBILITY TINTED LENS BLANK AND HORIZON 55...

K992010 · LPL

Ophthalmic · 14d

Cleared Dec 20, 1996

HORIZON/WESTHIN 38 SOFBLU (POLYMACON) SOFT (SPHERICAL & TORIC) DAILY WEAR...

W-55 (METHAFILON A) CONTACT LENS

K954524 · LPL

Ophthalmic · 181d

Cleared Mar 21, 1995

HORIZON 55 BI-CON TORIC

Westcon Contact Lens Co., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Westcon Contact Lens Co., Inc.

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