FDA applicant

Kelleher Corp.

Mchenry, IL94 decisions1982–19831 recall

FDA records 94 decisions for Kelleher Corp. (Mchenry, IL) from 1982 to 1983: 94 510(k) clearances. Most are in product codes EQN (Laryngoscope, Nasopharyngoscope) and KTG (Knife, Ent). 1 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 Kelleher Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kelleher Corp. since 2007.

Recalls per year

1in 2012

2007high 1 (2012) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Kelleher 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

Kelleher Corp.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?