FDA applicant
Zeus Scientific, Inc. (Zeus)
FDA records 1 decision for Zeus Scientific, Inc. (Zeus) (Raritan, NJ) in 2010: 1 510(k) clearance. All are in product code LIP (Enzyme Linked Immunoabsorption Assay…). 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 Zeus Scientific, Inc. (Zeus)’s devices, and how often a recall has named them.
FDA decisions per year
1in 2010
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2010.
Planning a device like Zeus Scientific, Inc. (Zeus)’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 “Zeus”
FDA records each applicant name separately; these may or may not be the same firm.