FDA applicant

Suqian Green Glove Co., Ltd.

Beijing, CN2 decisions2006–20060 recalls

FDA records 2 decisions for Suqian Green Glove Co., Ltd. (Beijing, CN) in 2006: 2 510(k) clearances. All are in product code LYZ (Vinyl Patient Examination Glove). Its devices cite 2 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 Suqian Green Glove Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Suqian Green Glove Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Suqian Green Glove Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Suqian Green Glove Co., Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Suqian”

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

Suqian Ruijang Medical Supplies Co., Ltd. 4 Suqian Xingye Glove Co,Ltd 2 Suqian Clean Glove Co., Ltd. 1 Suqian Linglian Medical Technology Co., Ltd. 1

Suqian Green Glove Co., Ltd.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Suqian”