FDA applicant

Zeus Technologies

Mchenry, IL5 decisions1983–19880 recalls

FDA records 5 decisions for Zeus Technologies (Mchenry, IL) from 1983 to 1988: 4 510(k) clearances and 1 original PMA approval. Most are in product codes LHL (Reagents, Antibody, Legionella, Direct &…) and JWX (Kit, Screening, Staphylococcus Aureus). 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 Zeus Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Zeus Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Zeus”

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

Zeus Scientific, Inc. 145 Zeus Scientific, Inc. (Zeus) 1

Zeus Technologies

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Zeus”