FDA applicant
Odin Medical Technologies, Ltd.
FDA records 5 decisions for Odin Medical Technologies, Ltd. (Yokneam Elit, IL) from 2001 to 2005: 5 510(k) clearances. Most are in product codes LNH (System, Nuclear Magnetic Resonance Imaging) and MOS (Coil, Magnetic Resonance, Specialty). Its devices cite 5 predicates, 2 of them its own earlier devices. 3 recalls are linked to its devices, 1 Class I.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Odin Medical Technologies, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Odin Medical Technologies, Ltd. since 2007.
Recalls per year
1in 2016
Class I Class II/III not classified
Planning a device like Odin Medical Technologies, Ltd.’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) ReportOther applicant names beginning “Odin”
FDA records each applicant name separately; these may or may not be the same firm.