510(k) Report

FDA applicant

Intavent Intl. S.A.

England, GB1 decision1991–19910 recalls

FDA records 1 decision for Intavent Intl. S.A. (England, GB) in 1991: 1 510(k) clearance. All are in product code CAE (Airway, Oropharyngeal, Anesthesiology). 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 Intavent Intl. S.A.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Intavent Intl. S.A. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • CAEAirway, Oropharyngeal, Anesthesiology1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K904834Intavent Laryngeal MaskIntavent Intl. S.A. · 19911cites it

What has FDA decided for it lately?

  • K904834Intavent Laryngeal MaskIntavent Intl. S.A. · 1991

The one decision as Intavent Intl. S.A. →