# Codi International BV

- Location (FDA's records): Boston, MA
- FDA decisions: 2 (1996–1996): 2 510(k) clearances
- Product codes: EFQ (2)
- 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
- K963188: Drain/Slit Sponge (Non-Sterile and Sterile) (Oct 30, 1996)
- K961061: Codi Synthetic Sponge (Non-Sterile and Sterile) (Jun 6, 1996)

Source page: https://510kreport.com/company/codi-international