FDA applicant

Somatics, Inc.

Lake Bluff, IL7 decisions1984–19990 recalls

FDA records 7 decisions for Somatics, Inc. (Lake Bluff, IL) from 1984 to 1999: 7 510(k) clearances. Most are in product codes QGH (Electroconvulsive Therapy Device For…) and JXL (Block, Bite). 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 Somatics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Somatics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Somatics, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?