510(k) Report

FDA applicant

Xuzhou Full Sun Medical Products, Ltd.

Jiangsu, CN8 decisions2007–20220 recalls

FDA records 8 decisions for Xuzhou Full Sun Medical Products, Ltd. (Jiangsu, CN) from 2007 to 2022: 8 510(k) clearances. Most are in product codes LYZ (Vinyl Patient Examination Glove) and LZA (Polymer Patient Examination Glove). Its devices cite 8 predicates, 0 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, general hospital panel, where it files most

How often FDA has decided Xuzhou Full Sun Medical Products, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2007: 62011: 12022: 1
2007high 6 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Xuzhou Full Sun Medical Products, Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Xuzhou Full Sun Medical Products, 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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Other applicant names beginning “Xuzhou”

FDA records each applicant name separately; these may or may not be the same firm.