# Ivent Corp.

- Location (FDA's records): Carlsbad, CA
- FDA decisions: 3 (1983–1985): 3 510(k) clearances
- Product codes: LDR (2), FPA (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
- K852259: Ivent Intravenous Adminstration Set (Jun 7, 1985)
- K842210: Ivent 302VC Dual Controller (Jul 25, 1984)
- K833953: Electronic Gravity 300VC (Dec 29, 1983)

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