FDA applicant

Siegen Corp.

Mountain View, CA6 decisions1984–19870 recalls

FDA records 6 decisions for Siegen Corp. (Mountain View, CA) from 1984 to 1987: 6 510(k) clearances. Most are in product codes GWF (Stimulator, Electrical, Evoked Response) and GXY (Electrode, Cutaneous). 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, neurology panel, where it files most

How often FDA has decided Siegen Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Siegen Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Siegen Corp.

Which product codes does it file in?

What has FDA decided for it lately?