# Ivion Corp.

- Location (FDA's records): Broomfield, CO
- FDA decisions: 3 (1992–1993): 3 510(k) clearances
- Product codes: FPA (1), LJT (1), FRN (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
- K925311: Trilogy Infusion Pump (Aug 16, 1993)
- K925219: Ivion Admin Sets W/Flow Clips (Jul 27, 1993)
- K920036: Surecath Port Access Catheter (Nov 25, 1992)

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