FDA applicant

Est International Corporation

Rancho Cucamonga, CA4 decisions2003–20040 recalls

FDA records 4 decisions for Est International Corporation (Rancho Cucamonga, CA) from 2003 to 2004: 4 510(k) clearances. All are in product code LYZ (Vinyl 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, general hospital panel, where it files most

How often FDA has decided Est International Corporation’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Est International Corporation since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Est International Corporation’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

Est International Corporation

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?