FDA applicant

Klafs Sunlight Corp.

Mchenry, IL3 decisions1981–19870 recalls

FDA records 3 decisions for Klafs Sunlight Corp. (Mchenry, IL) from 1981 to 1987: 3 510(k) clearances. All are in product code FTC (Light, Ultraviolet, Dermatological). 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 Klafs Sunlight Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Klafs Sunlight Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Klafs Sunlight Corp.

Which product codes does it file in?

What has FDA decided for it lately?