Zirconia Silicate Bead IOL Tumble Polishing

No FDA recalls found in the data synced 6 Oct 2026.

Trade Name

Optiflex Anterior Chamber Lenses (L1-L5)

Generic Name

intraocular lens

PMA Number

P820035 ↗

FDA Product Code

HQL

Device Class

Class III

Regulation

21 CFR Part 886.3600

Advisory Committee

Ophthalmic

FDA Decision

APWD Approval withdrawn

• Alcon Vision System

  Class II

  FDA 510(k) K063583 Active Cleared 9 May 2008

• Opti-Free Express Multi-Purpose Solution

  Class II

  FDA 510(k) K981574 Active Cleared 6 Jul 1998

• Inteliport Occluding Device

  Unclassified

  FDA 510(k) K040231 Active Cleared 13 Jul 2004

• Soft (Hydrophilic) Contact Lens Care Solution

  Class II

  FDA 510(k) K031193 Active Cleared 3 Jul 2003

• Alcon Multi-Purpose Solution

  Class II

  FDA 510(k) K071236 Active Cleared 12 Dec 2007

• Models 1S & 1P Intraocular Lens

  Class III

  FDA PMA P800049 Active Approved 31 Mar 1983

See all devices from Alcon →