FDA applicant

Drug Detection Devices, Ltd.

Alpharetta, GA8 decisions1999–20000 recalls

FDA records 8 decisions for Drug Detection Devices, Ltd. (Alpharetta, GA) from 1999 to 2000: 8 510(k) clearances. Most are in product codes DIS (Enzyme Immunoassay, Barbiturate) and DJG (Enzyme Immunoassay, Opiates). 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, clinical toxicology panel, where it files most

How often FDA has decided Drug Detection Devices, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Drug Detection Devices, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Drug”

FDA records each applicant name separately; these may or may not be the same firm.

Drug Screening Systems, Inc. 8 Drug Free Enterprises 1

Drug Detection Devices, Ltd.

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?

Other applicant names beginning “Drug”