FDA applicant

Denrick Corp.

Honolulu, HI1 decision1993–19930 recalls

FDA records 1 decision for Denrick Corp. (Honolulu, HI) in 1993: 1 510(k) clearance. All are in product code ESE (Larynx, Artificial (Battery-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, ear, nose and throat panel, where it files most

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

FDA decisions per year

No FDA decision for Denrick Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Denrick 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

Denrick Corp.

Which product codes does it file in?

What has FDA decided for it lately?