FDA applicant

Shizai Corp.

Mchenry, IL2 decisions1983–19830 recalls

FDA records 2 decisions for Shizai Corp. (Mchenry, IL) in 1983: 2 510(k) clearances. Most are in product codes KIF (Resin, Root Canal Filling) and EKA (File, Margin Finishing, Operative). 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 Shizai Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Shizai Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Shizai Corp.

Which product codes does it file in?

What has FDA decided for it lately?