FDA applicant

Westar Medical Products, Inc.

Mukilteo, WA1 decision2008–20080 recalls

FDA records 1 decision for Westar Medical Products, Inc. (Mukilteo, WA) in 2008: 1 510(k) clearance. All are in product code EIA (Unit, Operative Dental). 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 Westar Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2008high 1 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Westar Medical Products, Inc. by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Westar Medical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?