FDA applicant

Omnimedical

Mchenry, IL6 decisions1979–19830 recalls

FDA records 6 decisions for Omnimedical (Mchenry, IL) from 1979 to 1983: 6 510(k) clearances. Most are in product codes JAK (System, X-Ray, Tomography, Computed) and IZL (System, X-Ray, Mobile). 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Omnimedical since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Omnimedical”

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

Omnimedical Services, Inc. 1

Omnimedical

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Omnimedical”