510(k) Report

FDA applicant

Kaye Products, Inc.

Mchenry, IL12 decisions1979–19930 recalls

FDA records 12 decisions for Kaye Products, Inc. (Mchenry, IL) from 1979 to 1993: 12 510(k) clearances. Most are in product codes INN (Chair, Adjustable, Mechanical) and ILS (Adaptor, Hygiene). 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 Kaye Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kaye Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Kaye Products, Inc.’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