510(k) Report

FDA applicant

Kolberg Ocular Products, Inc.

San Diego, CA1 decision1995–19950 recalls

FDA records 1 decision for Kolberg Ocular Products, Inc. (San Diego, CA) in 1995: 1 510(k) clearance. All are in product code HQN (Conformer, 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 Kolberg Ocular Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kolberg Ocular Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Kolberg Ocular Products, Inc. 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?

  • HQNConformer, Ophthalmic1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K945110Kolberg Ophthalmic ConformerKolberg Ocular Products, Inc. · 19951cites it

What has FDA decided for it lately?

  • K945110Kolberg Ophthalmic ConformerKolberg Ocular Products, Inc. · 1995

The one decision as Kolberg Ocular Products, Inc. →