FDA applicant

American Technology, Inc.

Mchenry, IL3 decisions1977–19780 recalls

FDA records 3 decisions for American Technology, Inc. (Mchenry, IL) from 1977 to 1978: 3 510(k) clearances. All are in product code DTB (Permanent Pacemaker Electrode). 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, cardiovascular panel, where it files most

How often FDA has decided American Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for American Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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American Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?