510(k) Report

FDA applicant

Kaylight Corporation

Woodbury, CT1 decision2004–20040 recalls

FDA records 1 decision for Kaylight Corporation (Woodbury, CT) in 2004: 1 510(k) clearance. All are in product code ILY (Lamp, Infrared, Therapeutic Heating). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Kaylight Corporation since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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