FDA applicant

Kenlor Industries, Inc.

Westminster, CA9 decisions1989–19970 recalls

FDA records 9 decisions for Kenlor Industries, Inc. (Westminster, CA) from 1989 to 1997: 9 510(k) clearances. Most are in product codes JJY (Multi-Analyte Controls, All Kinds (Assayed)) and JJW (Urinalysis Controls (Assayed And Unassayed)). 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 Kenlor Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kenlor Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Kenlor Industries, 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?