510(k) Report

FDA applicant

Dentco, Inc.

White Plains, NY1 decision1995–19950 recalls

FDA records 1 decision for Dentco, Inc. (White Plains, NY) in 1995: 1 510(k) clearance. All are in product code EIS (Remover, Crown). 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 Dentco, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dentco, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Dentco, Inc.’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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