FDA applicant

Canyon Diagnostics, Inc.

Anaheim, CA9 decisions1985–19970 recalls

FDA records 9 decisions for Canyon Diagnostics, Inc. (Anaheim, CA) from 1985 to 1997: 9 510(k) clearances. Most are in product codes JJY (Multi-Analyte Controls, All Kinds (Assayed)) and IAF (Wright'S Stain). 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, clinical chemistry panel, where it files most

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

FDA decisions per year

No FDA decision for Canyon Diagnostics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Canyon Diagnostics, Inc.’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 Medical, Inc. 6 Canyon Medical Products 3

Canyon Diagnostics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Canyon”