# Orange Medical Instruments, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 12 (1982–1986): 12 510(k) clearances
- Product codes: FMF (3), CGA (3), CCE (2), KMK (1), FRN (1), FMI (1), JJX (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
- K860808: Continucath (Mar 13, 1986)
- K851822: Beta Scan Trends Meter (Oct 3, 1985)
- K844796: Micro-Beta U100 Syringe (Dec 18, 1984)
- K843882: Trends Lancet (Nov 5, 1984)
- K841369: Beta Scan Drystix (Aug 23, 1984)
- K833705: Betaject BD U100 (May 9, 1984)
- K833706: Click-Count U100 Insulin Syringe (Apr 5, 1984)
- K832691: Beta Scan Reagent Strip (Nov 14, 1983)

Source page: https://510kreport.com/company/orange-medical-instruments