FDA applicant

Trudell Medical

London, CA3 decisions1989–19990 recalls

FDA records 3 decisions for Trudell Medical (London, CA) from 1989 to 1999: 3 510(k) clearances. Most are in product codes CAF (Nebulizer (Direct Patient Interface)) and CAP (Monitor, Airway Pressure (Includes Gauge…). 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 Trudell Medical’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Trudell Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Trudell”

FDA records each applicant name separately; these may or may not be the same firm.

Trudell Medical Intl. 12 Trudell Medical International 9 Trudell Medical Int'L 3

Trudell Medical

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Trudell”