W-55 (Methafilcon a) Clear and Visibility Tinted Lens Blank and Horizon 55 Soft (Clear) and Horizon 55 Westint (Tinted)

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K992010 ↗

FDA Product Code

LPL

Device Class

Class II

Regulation

21 CFR Part 886.5925

Advisory Committee

Ophthalmic

FDA Decision

SESE Substantially Equivalent

• Horizon 55 Bi-Con

  Class II

  FDA 510(k) K945365 Active Cleared 28 Dec 1994

• Horizon 55 Bi-Con Toric

  Class II

  FDA 510(k) K950818 Active Cleared 21 Mar 1995

• Horizon 59 Oasis (Hioxifilcon a) Daily Wear Contact Lenses

  Class II

  FDA 510(k) K043540 Active Cleared 1 Feb 2005

• Horizon/Westhin 38 Sofblu (Polymacon) Soft (Spherical & Toric) Daily Wear Contact Lens (Tinted, Lathe-Cut From Lens Blan

  Class II

  FDA 510(k) K963837 Active Cleared 20 Dec 1996

• Horizon 38 (Clear) and Horizon 38 Westint (Tinted)

  Class II

  FDA 510(k) K023530 Active Cleared 26 Nov 2002

• Horizon (Methafilcon a) Daily Wear Sphere and Toric Contact Lenses

  Class II

  FDA 510(k) K031774 Active Cleared 20 Feb 2004

See all devices from Westcon Contact Lens Co., Inc. →