510(k) Report

FDA applicant

Richardson Merrel, Inc.

Mchenry, IL2 decisions1978–19790 recalls

FDA records 2 decisions for Richardson Merrel, Inc. (Mchenry, IL) from 1978 to 1979: 2 510(k) clearances. Most are in product codes EBE (Coating, Denture Hydrophilic, Resin) and JER (Cleaner, Denture, Mechanical). 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, dental panel, where it files most

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

FDA decisions per year

No FDA decision for Richardson Merrel, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • EBECoating, Denture Hydrophilic, Resin1decision
  • JERCleaner, Denture, Mechanical1decision

What has FDA decided for it lately?

  • K790339Concept IIRichardson Merrel, Inc. · 1979
  • K780254Denture Cleanser & Toothpaste in OneRichardson Merrel, Inc. · 1978

All 2 as Richardson Merrel, Inc. →

Other applicant names beginning “Richardson”

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

Richardson-Vicks, Inc. 1Richardson Scientific, Inc. 1