510(k) Report

FDA applicant

Microptics Development Laboratory

Newport Beach, CA1 decision1992–19920 recalls

FDA records 1 decision for Microptics Development Laboratory (Newport Beach, CA) in 1992: 1 510(k) clearance. All are in product code HNN (Knife, Ophthalmic). 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 Microptics Development Laboratory’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Microptics Development Laboratory since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Microptics Development Laboratory 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?

  • HNNKnife, Ophthalmic1decision

What has FDA decided for it lately?

  • K922378Ophthalmic KnifeMicroptics Development Laboratory · 1992

The one decision as Microptics Development Laboratory →