FDA applicant

Westport Medical, Inc.

Salem, OR1 decision2006–20060 recalls

FDA records 1 decision for Westport Medical, Inc. (Salem, OR) in 2006: 1 510(k) clearance. All are in product code EKX (Handpiece, Direct Drive, Ac-Powered). 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, dental panel, where it files most

How often FDA has decided Westport Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Westport Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Westport”

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

Westport Mobility Products, Inc. 1 Westport Pharmaceuticals, Inc. 1

Westport Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Westport”