FDA applicant

Dexall Biomedical Labs, Inc.

Gaithersburg, MD4 decisions1985–19890 recalls

FDA records 4 decisions for Dexall Biomedical Labs, Inc. (Gaithersburg, MD) from 1985 to 1989: 4 510(k) clearances. Most are in product codes DHB (System, Test, Radioallergosorbent (Rast)…) and DGO (Ige, Peroxidase, Antigen, Antiserum, Control). 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, immunology panel, where it files most

How often FDA has decided Dexall Biomedical Labs, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dexall Biomedical Labs, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dexall Biomedical Labs, Inc.

Which product codes does it file in?

What has FDA decided for it lately?