Softmark Contact Lens Identification System

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

Full name

Softmark

Generic Name

System, identification, contact lens

PMA Number

P820027 ↗

FDA Product Code

LOH

Device Class

Class III

Advisory Committee

Ophthalmic

FDA Decision

APWD Approval withdrawn

• Focus Dailies Visitint (Nelfilcon a) One-Day Contact Lens

  Class II

  FDA 510(k) K984273 Active Cleared 25 Jan 1999

• Aquify Lens Comfort Drops

  Class II

  FDA 510(k) K042176 Active Cleared 3 Nov 2004

• Glitter Eyes (Tefilcon) Soft (Hydrophilic) Contact Lens for Daily Wear

  Class II

  FDA 510(k) K003071 Active Cleared 13 Dec 2000

• Aosept Plus Cleaning and Disinfecting Solution

  Class II

  FDA 510(k) K003345 Active Cleared 26 Mar 2001

• Aosept Clear Care Cleaning and Disinfecting Solution

  Class II

  FDA 510(k) K023455 Active Cleared 28 Feb 2003

• Modification to Karats Multi-Purpose Solution

  Class II

  FDA 510(k) K031957 Active Cleared 14 Aug 2003

See all devices from Ciba Vision Corporation →