FDA applicant
Omikron Scientific, Ltd.
FDA records 4 decisions for Omikron Scientific, Ltd. (Israel, IL) from 1984 to 1991: 4 510(k) clearances. Most are in product codes KGX (Tape And Bandage, Adhesive) and DXG (Computer, Diagnostic, Pre-Programmed…). 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 Omikron Scientific, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Omikron Scientific, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Omikron Scientific, Ltd.’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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