510(k) Report

FDA applicant

Advanced Vision Science

Goleta, CA3 decisions1985–20000 recalls

FDA records 3 decisions for Advanced Vision Science (Goleta, CA) from 1985 to 2000: 2 510(k) clearances and 1 original PMA approval. Most are in product codes LZU (Plug, Punctum) and HQL (Intraocular Lens). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, ophthalmic panel, where it files most

How often FDA has decided Advanced Vision Science’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Advanced Vision Science since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Advanced Vision Science by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • LZUPlug, Punctum2decisions
  • HQLIntraocular Lens1decision

What has FDA decided for it lately?

  • K001234Bioinsulated Silicone Punctum PlugAdvanced Vision Science · 2000
  • K980844Surgidev Silicone Punctum PlugAdvanced Vision Science · 1998
  • P830033Style 17 & 17A Posterior Chamber IolsAdvanced Vision Science · 1985

All 3 as Advanced Vision Science →