FDA applicant

Philips Lighting Co.

Somerset, NJ7 decisions1991–20130 recalls

FDA records 7 decisions for Philips Lighting Co. (Somerset, NJ) from 1991 to 2013: 7 510(k) clearances. Most are in product codes FTC (Light, Ultraviolet, Dermatological) and LEJ (Booth, Sun Tan). No recall is linked to its devices.

FDA’s records also spell it “Philips Lighting Company”.

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 Philips Lighting Co.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2007high 1 (2013) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Philips Lighting Co.

Which product codes does it file in?

What has FDA decided for it lately?