FDA applicant

Cogan Corp.

Portland, OR1 decision1992–19920 recalls

FDA records 1 decision for Cogan Corp. (Portland, OR) in 1992: 1 510(k) clearance. All are in product code EGG (Attachment, Precision, All). 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, dental panel, where it files most

How often FDA has decided Cogan Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cogan Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Cogan Corp.’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

Cogan Corp.

Which product codes does it file in?

What has FDA decided for it lately?