510(k) Report

FDA applicant

The Cheney Co.

New Berlin, WI4 decisions1989–19900 recalls

FDA records 4 decisions for The Cheney Co. (New Berlin, WI) from 1989 to 1990: 4 510(k) clearances. Most are in product codes ING (Elevator, Wheelchair, Portable) and ILK (Transport, Patient, 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, physical medicine panel, where it files most

How often FDA has decided The Cheney Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Cheney Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like The Cheney Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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