FDA applicant

Biomedia, Inc.

Mchenry, IL19 decisions1979–19820 recalls

FDA records 19 decisions for Biomedia, Inc. (Mchenry, IL) from 1979 to 1982: 19 510(k) clearances. Most are in product codes JSI (Culture Media, Selective And Differential) and JTZ (Culture Media, Antimicrobial Susceptibility…). 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 Biomedia, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Biomedia, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Biomedia, Inc.

Which product codes does it file in?

What has FDA decided for it lately?