FDA applicant

Unimetrics Corp.

Mchenry, IL2 decisions1976–19770 recalls

FDA records 2 decisions for Unimetrics Corp. (Mchenry, IL) from 1976 to 1977: 2 510(k) clearances. Most are in product codes EOQ (Bronchoscope (Flexible Or Rigid)) and DXL (Injector, Indicator). 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, ear, nose and throat panel, where it files most

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

FDA decisions per year

No FDA decision for Unimetrics Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Unimetrics Corp.

Which product codes does it file in?

What has FDA decided for it lately?