FDA applicant

American Design Group, Inc.

Concord, CA3 decisions1989–19910 recalls

FDA records 3 decisions for American Design Group, Inc. (Concord, CA) from 1989 to 1991: 3 510(k) clearances. Most are in product codes LZN (Cement Obturator) and GDM (Needle, Aspiration And Injection, Reusable). 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 American Design Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for American Design Group, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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American Design Group, Inc.

Which product codes does it file in?

What has FDA decided for it lately?