FDA applicant

Whitehall Laboratories, Inc.

New York, NY2 decisions1988–19890 recalls

FDA records 2 decisions for Whitehall Laboratories, Inc. (New York, NY) from 1988 to 1989: 2 510(k) clearances. Most are in product codes EFW (Toothbrush, Manual) and JES (Floss, Dental). 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 Whitehall Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Whitehall Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Whitehall Laboratories, 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 “Whitehall”

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

Whitehall/Div Columbus Mckennon Corp. 1

Whitehall Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Whitehall”