FDA applicant

Westmed Intl.

Tucson, AZ9 decisions1993–19960 recalls

FDA records 9 decisions for Westmed Intl. (Tucson, AZ) from 1993 to 1996: 9 510(k) clearances. Most are in product codes CAH (Filter, Bacterial, Breathing-Circuit) and BTI (Compressor, Air, Portable). 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 Westmed Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Westmed Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Westmed”

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

Westmed, Inc. 8

Westmed Intl.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Westmed”