FDA applicant
Silverman'S
FDA records 2 decisions for Silverman'S (Mchenry, IL) from 1980 to 1983: 2 510(k) clearances. Most are in product codes EIA (Unit, Operative Dental) and EAY (Light, Fiber Optic, Dental). 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 Silverman'S’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Silverman'S since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Silverman'S’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