510(k) Report

FDA applicant

Jeneric Ind.

Mchenry, IL25 decisions1982–19860 recalls

FDA records 25 decisions for Jeneric Ind. (Mchenry, IL) from 1982 to 1986: 25 510(k) clearances. Most are in product codes EJH (Alloy, Metal, Base) and EJS (Alloy, Other Noble Metal). 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 Jeneric Ind.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Jeneric Ind. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Jeneric”

FDA records each applicant name separately; these may or may not be the same firm.