FDA applicant

Stanford Professional Products

Mchenry, IL2 decisions1978–19790 recalls

FDA records 2 decisions for Stanford Professional Products (Mchenry, IL) from 1978 to 1979: 2 510(k) clearances. Most are in product codes FRG (Wrap, Sterilization) and GDY (Gauze/Sponge, Internal, X-Ray Detectable). 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 hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Stanford Professional Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Stanford Professional Products’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Stanford”

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

Stanford Scientific, Inc. 4 Stanford Laboratories 2 Stanford Assoc., Inc. 2

Stanford Professional Products

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Stanford”