FDA applicant

The Richmond Light Co.

Walker, MI2 decisions1981–20050 recalls

FDA records 2 decisions for The Richmond Light Co. (Walker, MI) from 1981 to 2005: 2 510(k) clearances. All are in product code FTC (Light, Ultraviolet, Dermatological). Its devices cite 3 predicates, 1 of them its own earlier devices. 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 The Richmond Light Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Richmond Light Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like The Richmond Light Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “The”

FDA records each applicant name separately; these may or may not be the same firm.

Richmond Products, Inc. 15 Richmond Diagnostics, Inc. 1

The Richmond Light Co.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “The”