# Omikron Scientific, Ltd.

- Location (FDA's records): Israel, IL
- FDA decisions: 4 (1984–1991): 4 510(k) clearances
- Product codes: KGX (1), DXG (1), NAD (1), DXY (1)
- 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
- K904445: Omiband (Mar 6, 1991)
- K874480: Modified Manufacturing Process for Omiderm (TM) (Feb 22, 1988)
- K844277: Omikron Pacemaker 837 Unipolar & 838 Bipolar (Feb 15, 1985)
- K840748: Lithium Pacemaker 811-811L & 811XL (Aug 3, 1984)

Source page: https://510kreport.com/company/omikron-scientific