510(k) Report

FDA applicant

Silverman'S

Mchenry, IL2 decisions1980–19830 recalls

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, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

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.

FIG. 1 — Silverman'S by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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