510(k) Report

FDA applicant

Taidoc Technology Corporation

New Taipei City, TW123 decisions2004–20240 recalls

FDA records 123 decisions for Taidoc Technology Corporation (New Taipei City, TW) from 2004 to 2024: 123 510(k) clearances. Most are in product codes NBW (System, Test, Blood Glucose, Over The Counter) and FLL (Continuous Measurement Thermometer). Since 2016 its 510(k)s took a median of 241 days from receipt to decision, against 209 for FDA’s reviews in the same codes and years. Its devices cite 100 predicates, 66 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, clinical chemistry panel, where it files most

How often FDA has decided Taidoc Technology Corporation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2007: 82008: 162009: 162010: 222011: 162012: 82013: 52015: 22016: 42017: 12018: 72019: 22022: 22024: 1
2007high 22 (2010) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Taidoc Technology Corporation’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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