# Koi, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 7 (1981–1986): 7 510(k) clearances
- Product codes: HNN (2), HKL (1), ITX (1), HMX (1), HNW (1), HOE (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
- K843247: Koi Pachymeter (Apr 30, 1986)
- K830366: Diamond Knife (Mar 9, 1983)
- K812764: Koi Blue Field Entoptoscope (Dec 2, 1981)
- K812450: Koi Diamond Knife (Sep 21, 1981)
- K812097: Koi Lacremal Hook & Dilator (Aug 18, 1981)
- K812010: Koi Lacrimal Intubation System (Jul 28, 1981)
- K812011: Blade Gauge (Jul 28, 1981)

Source page: https://510kreport.com/company/koi