FDA applicant

Vedi Corp.

Plano, TX1 decision2004–20040 recalls

FDA records 1 decision for Vedi Corp. (Plano, TX) in 2004: 1 510(k) clearance. All are in product code BTM (Ventilator, Emergency, Manual (Resuscitator)). 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, anesthesiology panel, where it files most

How often FDA has decided Vedi Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vedi Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Vedi Corp.

Which product codes does it file in?

What has FDA decided for it lately?