FDA applicant

Wen Hao, Inc.

Pasadena, CA5 decisions1989–19900 recalls

FDA records 5 decisions for Wen Hao, Inc. (Pasadena, CA) from 1989 to 1990: 5 510(k) clearances. Most are in product codes EKJ (Burnisher, Operative) and LYY (Latex 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, dental panel, where it files most

How often FDA has decided Wen Hao, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Wen Hao, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Wen Hao, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Wen Hao, Inc.

Which product codes does it file in?

What has FDA decided for it lately?