FDA applicant

Redwood Biotech, Inc.

Sunnyvale, CA6 decisions1999–20000 recalls

FDA records 6 decisions for Redwood Biotech, Inc. (Sunnyvale, CA) from 1999 to 2000: 6 510(k) clearances. Most are in product codes LAF (Gas Chromatography, Methamphetamine) and DIO (Enzyme Immunoassay, Cocaine And Cocaine…). 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 Redwood Biotech, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Redwood Biotech, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Redwood Biotech, Inc.

Which product codes does it file in?

What has FDA decided for it lately?