FDA applicant

Denley Instruments, Inc.

Bethesda, MD9 decisions1989–19920 recalls

FDA records 9 decisions for Denley Instruments, Inc. (Bethesda, MD) from 1989 to 1992: 9 510(k) clearances. Most are in product codes JQW (Station, Pipetting And Diluting, For Clinical…) and JJQ (Colorimeter, Photometer, Spectrophotometer For…). 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 Denley Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Denley Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Denley Instruments, 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?