FDA applicant

Utah Pioneer Medical, Inc.

Orem, UT2 decisions1992–19940 recalls

FDA records 2 decisions for Utah Pioneer Medical, Inc. (Orem, UT) from 1992 to 1994: 2 510(k) clearances. Most are in product codes GCA (Biliary Catheter For Stone Removal That May…) and GCJ (Laparoscope, General & Plastic Surgery). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Utah Pioneer Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Utah Pioneer Medical, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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 Bioresearch, Inc. 1 Utah Medical Products and Services 1

Utah Pioneer Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Utah”