FDA applicant
Gregory S. Jacob, D.D.S.
FDA records 1 decision for Gregory S. Jacob, D.D.S. (Des Plains, IL) in 2000: 1 510(k) clearance. All are in product code EBZ (Activator, Ultraviolet, For Polymerization). 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 Gregory S. Jacob, D.D.S.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Gregory S. Jacob, D.D.S. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Gregory S. Jacob, D.D.S.’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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