510(k) Report

FDA applicant

E-Care Technology Corporation

Chubei, TW3 decisions2002–20180 recalls

FDA records 3 decisions for E-Care Technology Corporation (Chubei, TW) from 2002 to 2018: 3 510(k) clearances. All are in product code FLL (Continuous Measurement Thermometer). Its devices cite 4 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “E-Care Technology Co., Ltd.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

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

FDA decisions per year

1in 2018

2012: 12018: 1
2007high 1 (2012) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like E-Care 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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