FDA applicant
Daxor Corporation
FDA records 4 decisions for Daxor Corporation (Oak Ridge, TN) from 1997 to 2026: 4 510(k) clearances. Most are in product codes JWO (Device, Blood Volume Measuring) and FMF (Syringe, Piston). Its devices cite 2 predicates, 2 of them its own earlier devices. 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 Daxor Corporation’s devices, and how often a recall has named them.
FDA decisions per year
1in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Daxor Corporation’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report