Specialty D-UV (Ocufilcon D) Soft (Hydrophilic) Contact Lens for Daily Wear, Specialty D-UV Multifocal (Ocuflicon D)

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

510(k) Number

K011542 ↗

FDA Product Code

LPL

Device Class

Class II

Regulation

21 CFR Part 886.5925

Advisory Committee

Ophthalmic

FDA Decision

SESE Substantially Equivalent

• Speciality 55 Multifocal (Methafilcon a) Soft (Hydrophilic) Contact Lenses for Daily Wear, Speciality 55 (Methafilcon a)

  Class II

  FDA 510(k) K984090 Active Cleared 7 Jul 1999

• Specialty Progressive(Methafilcon a)Multifocal Soft(Hydrophilic)Contact Lens for Daily Wear(Clear and Tinted)

  Class II

  FDA 510(k) K963488 Active Cleared 20 Nov 1996

• Specialty 55 UV (Methafilcon a) Soft (Hydrophilic) Contact Lens for Daily Wear, Specialty 55 UV Multifocal (Methafilcon)

  Class II

  FDA 510(k) K003526 Active Cleared 12 Feb 2001

• UltraCon/UltraCon S Rigid Gas Permeable Contact Lens for Daily Wear

  Class II

  FDA 510(k) K980197 Active Cleared 4 Aug 1998

• Epicon (Carbosilfocon a) Rigid Gas Permeable Contact Lens Daily Wear

  Class II

  FDA 510(k) K992787 Active Cleared 2 Feb 2000

• Specialty T Toric (Ocufilcon a) Contact Lens for Daily Wear

  Class II

  FDA 510(k) K963764 Active Cleared 30 Jan 1997

See all devices from Specialty Ultravision, Inc. →