FDA applicant
Kaye Products, Inc.
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
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.
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