FDA applicant

China National Medicines & Health Prod. I/E Corp.

Suite 500, Washington, DC12 decisions1987–19910 recalls

FDA records 12 decisions for China National Medicines & Health Prod. I/E Corp. (Suite 500, Washington, DC) from 1987 to 1991: 12 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and EFQ (Gauze/Sponge, Internal). 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 China National Medicines & Health Prod. I/E Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for China National Medicines & Health Prod. I/E Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — China National Medicines & Health Prod. I/E Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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China National Medicines & Health Prod. I/E Corp.

Which product codes does it file in?

What has FDA decided for it lately?