FDA applicant

Herbert Stanley Co.

Skokie, IL2 decisions1989–19890 recalls

FDA records 2 decisions for Herbert Stanley Co. (Skokie, IL) in 1989: 2 510(k) clearances. Most are in product codes JOT (Electrode, Gel, Electrosurgical) and DPS (Electrocardiograph). 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 Herbert Stanley Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Herbert Stanley Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Herbert Stanley Co.

Which product codes does it file in?

What has FDA decided for it lately?