FDA applicant

Hong DI Plastic Products Co., Ltd.

Chino, CA5 decisions2007–20100 recalls

FDA records 5 decisions for Hong DI Plastic Products Co., Ltd. (Chino, CA) from 2007 to 2010: 5 510(k) clearances. All are in product code LYZ (Vinyl Patient Examination Glove). Its devices cite 3 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 Hong DI Plastic Products Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

3in 2010

2007high 3 (2010) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Hong DI Plastic Products Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Hong DI Plastic Products 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 “Hong”

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

Hong Qiangxing (Shenzhen) Electronics Limited 10 Hong Seng Gloves Sdn Bhd 4 Hong Huang Tang Industrial Co., Ltd. 3 Hong YA Non-Woven Products Co., Ltd. 2 Hong Xin Rubber Products Co., Ltd. 1 Hong Kong Etech Groups Limited 1

Hong DI Plastic Products 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 “Hong”