510(k) Report

FDA applicant

Sylvania Lighting Products

Danvers, MA4 decisions1985–19850 recalls

FDA records 4 decisions for Sylvania Lighting Products (Danvers, MA) in 1985: 4 510(k) clearances. Most are in product codes FTC (Light, Ultraviolet, Dermatological) and KGL (Cabinet, Phototherapy (Puva)). 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 Sylvania Lighting Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sylvania Lighting Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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