FDA applicant

Larken Industries, Inc.

Lenexa, KS3 decisions1984–19870 recalls

FDA records 3 decisions for Larken Industries, Inc. (Lenexa, KS) from 1984 to 1987: 3 510(k) clearances. Most are in product codes JJQ (Colorimeter, Photometer, Spectrophotometer For…) and CGA (Glucose Oxidase, Glucose). 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 Larken Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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Larken Industries, Inc.

Which product codes does it file in?

What has FDA decided for it lately?