FDA applicant

Deseret Medical, Inc.

Sandy, UT20 decisions1979–19910 recalls

FDA records 20 decisions for Deseret Medical, Inc. (Sandy, UT) from 1979 to 1991: 20 510(k) clearances. Most are in product codes FOZ (Catheter, Intravascular, Therapeutic…) and FPA (Set, Administration, Intravascular). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Deseret Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Deseret”

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

Deseret Pharmaceutical Co. 1

Deseret Medical, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Deseret”