FDA applicant

Dw Industries, Inc.

Washington, DC2 decisions1992–19970 recalls

FDA records 2 decisions for Dw Industries, Inc. (Washington, DC) from 1992 to 1997: 2 510(k) clearances. Most are in product codes ECB (Unit, Syringe, Air And/Or Water) and EFB (Handpiece, Air-Powered, 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 Dw Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dw Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dw Industries, Inc.

Which product codes does it file in?

What has FDA decided for it lately?