510(k) Report

FDA applicant

Codent Technical Industry Co., Ltd.

Kaohsiung City, TW5 decisions2004–20240 recalls

FDA records 5 decisions for Codent Technical Industry Co., Ltd. (Kaohsiung City, TW) from 2004 to 2024: 5 510(k) clearances. Most are in product codes EFB (Handpiece, Air-Powered, Dental) and EBW (Controller, Foot, Handpiece And Cord). Its devices cite 9 predicates, 2 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 Codent Technical Industry Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2014: 12015: 22024: 1
2007high 2 (2015) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Codent Technical Industry 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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