FDA applicant

Whitney Products, Inc.

Glenview, IL1 decision1994–19940 recalls

FDA records 1 decision for Whitney Products, Inc. (Glenview, IL) in 1994: 1 510(k) clearance. All are in product code FZS (Curette, Surgical, General Use). 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 Whitney Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Whitney 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 “Whitney”

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

Whitney Medical Solutions 1

Whitney Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Whitney”