FDA applicant
A.B. Dental Devices, Ltd.
FDA records 4 decisions for A.B. Dental Devices, Ltd. (M.P. Misgav, IL) from 2006 to 2026: 4 510(k) clearances. All are in product code DZE (Implant, Endosseous, Root-Form). Its devices cite 30 predicates, 3 of them its own earlier devices. 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 A.B. Dental Devices, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2014
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like A.B. Dental Devices, 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) Report