FDA applicant

Canberra Industries, Inc.

Meriden, CT3 decisions1983–19930 recalls

FDA records 3 decisions for Canberra Industries, Inc. (Meriden, CT) from 1983 to 1993: 3 510(k) clearances. Most are in product codes JZD (Snare, Ear) and JJJ (Counter (Beta, Gamma) For Clinical Use). 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, ear, nose and throat panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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Canberra Industries, Inc.

Which product codes does it file in?

What has FDA decided for it lately?