FDA applicant

Richmond Products, Inc.

Boca Raton, FL15 decisions1987–19880 recalls

FDA records 15 decisions for Richmond Products, Inc. (Boca Raton, FL) from 1987 to 1988: 15 510(k) clearances. Most are in product codes HIT (Tester, Color Vision) and HLP (Target, Fusion And Stereoscopic). 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, ophthalmic panel, where it files most

How often FDA has decided Richmond Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Richmond Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Richmond”

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

The Richmond Light Co. 2 Richmond Diagnostics, Inc. 1

Richmond Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Richmond”