510(k) Report

FDA applicant

Jda (Tianjin) Plastic Rubber Co., Ltd.

Beijing 100022, CN1 decision2003–20030 recalls

FDA records 1 decision for Jda (Tianjin) Plastic Rubber Co., Ltd. (Beijing 100022, CN) in 2003: 1 510(k) clearance. All are in product code LZA (Polymer Patient Examination Glove). Its devices cite 1 predicate, 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 Jda (Tianjin) Plastic Rubber Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Jda (Tianjin) Plastic Rubber Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Jda (Tianjin) Plastic Rubber Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Jda (Tianjin) Plastic Rubber 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

Which product codes does it file in?

  • LZAPolymer Patient Examination Glove1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K030529Legend (Brand) Nitrile Powder-Free Patient Examination GloveJda (Tianjin) Plastic Rubber Co., Ltd. · 2003

The one decision as Jda (Tianjin) Plastic Rubber Co., Ltd. →