510(k) Report

FDA applicant

Ech (Changzhou) Medical Instrument Co., Ltd.

Changzhou, CN1 decision2017–20170 recalls

FDA records 1 decision for Ech (Changzhou) Medical Instrument Co., Ltd. (Changzhou, CN) in 2017: 1 510(k) clearance. All are in product code FLL (Continuous Measurement Thermometer). 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, general hospital panel, where it files most

How often FDA has decided Ech (Changzhou) Medical Instrument Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2017: 1
2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Ech (Changzhou) Medical Instrument Co., Ltd. by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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