FDA applicant

Dpm USA Corp.

Miami, FL2 decisions2009–20090 recalls

FDA records 2 decisions for Dpm USA Corp. (Miami, FL) in 2009: 2 510(k) clearances. Most are in product codes ELC (Scaler, Ultrasonic) and EFA (Handpiece, Belt And/Or Gear Driven, Dental). Its devices cite 2 predicates, 0 of them its own earlier devices. 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 Dpm USA Corp.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2009

2009high 2 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Dpm USA Corp. by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Dpm USA Corp.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?