510(k) Report

FDA applicant

Vipi Industria,Comercio,Exportacao E Importacao DE

Greenwood Village, CO1 decision2010–20100 recalls

FDA records 1 decision for Vipi Industria,Comercio,Exportacao E Importacao DE (Greenwood Village, CO) in 2010: 1 510(k) clearance. All are in product code EBG (Crown And Bridge, Temporary, Resin). 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 Vipi Industria,Comercio,Exportacao E Importacao DE’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2010: 1
2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Vipi Industria,Comercio,Exportacao E Importacao DE by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • EBGCrown And Bridge, Temporary, Resin1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K102341Vipi BlockVipi Industria,Comercio,Exportacao E Importacao DE · 20101cites it

What has FDA decided for it lately?

  • K102341Vipi BlockVipi Industria,Comercio,Exportacao E Importacao DE · 2010

The one decision as Vipi Industria,Comercio,Exportacao E Importacao DE →