FDA applicant

Utah Bioresearch, Inc.

Salt Lake City, UT1 decision1988–19880 recalls

FDA records 1 decision for Utah Bioresearch, Inc. (Salt Lake City, UT) in 1988: 1 510(k) clearance. All are in product code GPG (Antigen, Latex Agglutination, Trichinella…). 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 Utah Bioresearch, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Utah Bioresearch, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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See the 510(k) Report

Other applicant names beginning “Utah”

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

Utah Medical Products, Inc. 38 Utah Pioneer Medical, Inc. 2 Utah Medical Products and Services 1

Utah Bioresearch, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Utah”