FDA applicant

Ivent Corp.

Carlsbad, CA3 decisions1983–19850 recalls

FDA records 3 decisions for Ivent Corp. (Carlsbad, CA) from 1983 to 1985: 3 510(k) clearances. Most are in product codes LDR (Controller, Infusion, Intravascular, Electronic) and FPA (Set, Administration, Intravascular). 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 Ivent Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ivent Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ivent Corp.

Which product codes does it file in?

What has FDA decided for it lately?