510(k) Report

FDA applicant

Stick Tech, Ltd.

Mount Vernon, NY9 decisions2001–20060 recalls

FDA records 9 decisions for Stick Tech, Ltd. (Mount Vernon, NY) from 2001 to 2006: 9 510(k) clearances. Most are in product codes EBI (Resin, Denture, Relining, Repairing, Rebasing) and EBF (Material, Tooth Shade, Resin). Its devices cite 9 predicates, 6 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, last Nov 3, 2026

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

How often FDA has decided Stick Tech, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Stick Tech, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Stick Tech, 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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