510(k) Report

FDA applicant

Dental Suppliers of America, Inc.

Arlington, WA1 decision2006–20060 recalls

FDA records 1 decision for Dental Suppliers of America, Inc. (Arlington, WA) in 2006: 1 510(k) clearance. All are in product code EIH (Powder, Porcelain). 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 Dental Suppliers of America, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dental Suppliers of America, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Dental Suppliers of America, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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