FDA applicant

Clement Clarke, Inc.

England, GB10 decisions1979–19960 recalls

FDA records 10 decisions for Clement Clarke, Inc. (England, GB) from 1979 to 1996: 10 510(k) clearances. Most are in product codes BZH (Meter, Peak Flow, Spirometry) and HJO (Biomicroscope, Slit-Lamp, Ac-Powered). 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, ophthalmic panel, where it files most

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

FDA decisions per year

No FDA decision for Clement Clarke, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Clement”

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

Clement Clarke Intl., Ltd. 6

Clement Clarke, 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?

Other applicant names beginning “Clement”