510(k) Report

FDA applicant

Lever Brothers Company, Inc.

Edgewater, NJ4 decisions1978–19850 recalls

FDA records 4 decisions for Lever Brothers Company, Inc. (Edgewater, NJ) from 1978 to 1985: 4 510(k) clearances. Most are in product codes EFT (Cleanser, Denture, Over The Counter) and EBD (Coating, Filling Material, Resin). 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 Lever Brothers Company, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lever Brothers Company, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Lever Brothers Company, 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?

  • EFTCleanser, Denture, Over The Counter2decisions
  • EBDCoating, Filling Material, Resin1decision
  • EFWToothbrush, Manual1decision

What has FDA decided for it lately?

  • K850610Pepsodent Denture Adhesive CreamLever Brothers Company, Inc. · 1985
  • K851182Pepsodent Denture Cleanser-Westone FormulaLever Brothers Company, Inc. · 1985
  • K851183Pepsodent Denture Cleanser PDP FormulaLever Brothers Company, Inc. · 1985
  • K781018DX ToothbrushLever Brothers Company, Inc. · 1978

All 4 as Lever Brothers Company, Inc. →