FDA applicant
Codi International BV
FDA records 2 decisions for Codi International BV (Boston, MA) in 1996: 2 510(k) clearances. All are in product code EFQ (Gauze/Sponge, Internal). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Codi International BV’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Codi International BV since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Codi International BV’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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