FDA applicant

Lca, Inc.

Cincinnati, OH12 decisions1990–19950 recalls

FDA records 12 decisions for Lca, Inc. (Cincinnati, OH) from 1990 to 1995: 12 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and FYD (Apparatus, Exhaust, Surgical). 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, general and plastic surgery panel, where it files most

How often FDA has decided Lca, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lca, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Lca, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?