510(k) Report

FDA applicant

Fujian Jixiang Medical Technology Co.,Ltd

Longyan, CN1 decision2022–20220 recalls

FDA records 1 decision for Fujian Jixiang Medical Technology Co.,Ltd (Longyan, CN) in 2022: 1 510(k) clearance. All are in product code LZA (Polymer Patient Examination Glove). 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 Fujian Jixiang Medical Technology Co.,Ltd’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2022: 1
2022high 1 (2022) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — Fujian Jixiang Medical Technology Co.,Ltd by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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