FDA applicant

Wang Tong Xinghua Co., Ltd.

Xinghua, CN2 decisions2013–20130 recalls

FDA records 2 decisions for Wang Tong Xinghua Co., Ltd. (Xinghua, CN) in 2013: 2 510(k) clearances. All are in product code LYZ (Vinyl 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 Wang Tong Xinghua Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2013

2013high 2 (2013) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — Wang Tong Xinghua Co., Ltd. by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Wang Tong Xinghua 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 “Wang”

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

Wang & Li, Inc. 1

Wang Tong Xinghua Co., Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Wang”