FDA applicant

Canyon Medical Products

Salt Lake City, UT3 decisions1988–19950 recalls

FDA records 3 decisions for Canyon Medical Products (Salt Lake City, UT) from 1988 to 1995: 3 510(k) clearances. Most are in product codes DWF (Catheter, Cannula And Tubing, Vascular…) and KYX (Dispenser, Liquid Medication). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Canyon Medical Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Canyon”

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

Canyon Diagnostics, Inc. 9 Canyon Medical, Inc. 6

Canyon Medical Products

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Canyon”