FDA applicant
Alpha Omega, Ltd.
FDA records 5 decisions for Alpha Omega, Ltd. (Nazareth Illit, IL) from 2000 to 2007: 5 510(k) clearances. Most are in product codes GZL (Electrode, Depth) and DWC (Controller, Temperature, Cardiopulmonary Bypass). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Alpha Omega, Inc.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Alpha Omega, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2007
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Alpha Omega, 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 “Alpha”
FDA records each applicant name separately; these may or may not be the same firm.