FDA applicant

Lkc Technologies, Inc.

Gaithersburg, MD8 decisions1976–20150 recalls

FDA records 8 decisions for Lkc Technologies, Inc. (Gaithersburg, MD) from 1976 to 2015: 8 510(k) clearances. Most are in product codes HLX (Photostimulator, Ac-Powered) and HPT (Perimeter, Automatic, Ac-Powered). 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 Lkc Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2007high 1 (2015) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Lkc Technologies, 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?