FDA applicant

Neward Enterprises, Inc.

Cucamonga, CA8 decisions1984–19960 recalls

FDA records 8 decisions for Neward Enterprises, Inc. (Cucamonga, CA) from 1984 to 1996: 8 510(k) clearances. Most are in product codes HDB (Extractor, Vacuum, Fetal) and HGP (Electrode, Circular (Spiral), Scalp And…). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Neward Enterprises, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Neward Enterprises, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?