# Kaye Products, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 12 (1979–1993): 12 510(k) clearances
- Product codes: INN (3), ILS (1), FRP (1), LBE (1), IOD (1), ION (1), INM (1), IOR (1), ITJ (1), IOE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K924848: Kaye Scoot-About, Model SB1 (Feb 12, 1993)
- K923095: Kaye Model Kiao Pelvic/Thigh Stabilizer (Jul 21, 1992)
- K922061: Chair, Adjustable, Mechanical (May 26, 1992)
- K885330: Wheelchair, Mechanical (Feb 3, 1989)
- K833869: Child's Walker (Nov 29, 1983)
- K830560: Exerciser, Passive, Non Measuring (Mar 9, 1983)
- K830466: Bars, Parallel, Exercise (Mar 9, 1983)
- K820591: Mechanical Chair (Mar 15, 1982)

Source page: https://510kreport.com/company/kaye-products