FDA applicant

Uti-Tect, Inc.

Mchenry, IL3 decisions1981–19840 recalls

FDA records 3 decisions for Uti-Tect, Inc. (Mchenry, IL) from 1981 to 1984: 3 510(k) clearances. Most are in product codes JTZ (Culture Media, Antimicrobial Susceptibility…) and JTY (Culture Media, For Isolation Of Pathogenic…). 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 Uti-Tect, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Uti-Tect, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Uti-Tect, Inc.

Which product codes does it file in?

What has FDA decided for it lately?