FDA applicant

Cederroth, Inc. USA

Mchenry, IL7 decisions1982–19880 recalls

FDA records 7 decisions for Cederroth, Inc. USA (Mchenry, IL) from 1982 to 1988: 7 510(k) clearances. Most are in product codes KGX (Tape And Bandage, Adhesive) and FRO (Dressing, Wound, Drug). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Cederroth, Inc. USA since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Cederroth, Inc. USA’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

Cederroth, Inc. USA

Which product codes does it file in?

What has FDA decided for it lately?