FDA applicant

Dio Department Dsi, Inc.

Santa Fe Springs, CA8 decisions2006–20080 recalls

FDA records 8 decisions for Dio Department Dsi, Inc. (Santa Fe Springs, CA) from 2006 to 2008: 8 510(k) clearances. All are in product code DZE (Implant, Endosseous, Root-Form). Its devices cite 17 predicates, 3 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 Dio Department Dsi, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

5in 2008

2007high 5 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Dio Department Dsi, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?