FDA applicant

Id Biomedical Corp.

Bothell, WA3 decisions1999–20020 recalls

FDA records 3 decisions for Id Biomedical Corp. (Bothell, WA) from 1999 to 2002: 3 510(k) clearances. Most are in product codes MYI (System, Test, Genotypic Detection, Resistant…) and NIJ (System, Test, Genotypic Detection, Resistant…). Its devices cite 2 predicates, 0 of them its own earlier devices. 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, microbiology panel, where it files most

How often FDA has decided Id Biomedical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Id Biomedical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Id Biomedical Corp.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?