FDA applicant

Damon Corp.

Mchenry, IL11 decisions1976–19870 recalls

FDA records 11 decisions for Damon Corp. (Mchenry, IL) from 1976 to 1987: 11 510(k) clearances. Most are in product codes JQC (Centrifuges (Micro, Ultra, Refrigerated) For…) and LLZ (System, Image Processing, Radiological). 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, clinical chemistry panel, where it files most

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

FDA decisions per year

No FDA decision for Damon Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Damon 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

Damon Corp.

Which product codes does it file in?

What has FDA decided for it lately?