# Anodia Systems

- Location (FDA's records): Danville, KY
- FDA decisions: 4 (1993–2003): 4 510(k) clearances
- Product codes: EIA (3), EFB (1)
- Predicates its devices cite: 4 (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

## Firms whose devices it cites most
- A-Dec, Inc.: 3 (https://510kreport.com/company/a-dec)
- Steri-Sol, Inc.: 1 (https://510kreport.com/company/steri-sol)

## Recent decisions
- K023815: C-1805M (Jun 19, 2003)
- K023896: C-1890 (Jun 19, 2003)
- K023213: RDH-2000 (Jan 16, 2003)
- K925378: Steri-Sol Solution, Modification (Jul 22, 1993)

Source page: https://510kreport.com/company/anodia-systems
