FDA applicant
Toei Electric Co., Ltd.
FDA records 3 decisions for Toei Electric Co., Ltd. (Deer Field, IL) from 1997 to 2002: 3 510(k) clearances. Most are in product codes LQY (Locator, Root Apex) and EBZ (Activator, Ultraviolet, For Polymerization). Its devices cite 4 predicates, 1 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 Toei Electric Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Toei Electric Co., Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Toei Electric Co., Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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