FDA applicant

Stanford Laboratories

Mchenry, IL2 decisions1980–19810 recalls

FDA records 2 decisions for Stanford Laboratories (Mchenry, IL) from 1980 to 1981: 2 510(k) clearances. Most are in product codes GDY (Gauze/Sponge, Internal, X-Ray Detectable) and FMF (Syringe, Piston). 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 Stanford Laboratories’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Stanford Laboratories since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Stanford Laboratories’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 Assoc., Inc. 2 Stanford Professional Products 2

Stanford Laboratories

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Stanford”