510(k) Report

FDA applicant

Inovativ, LLC

Jefferson, OR3 decisions2002–20030 recalls

FDA records 3 decisions for Inovativ, LLC (Jefferson, OR) from 2002 to 2003: 3 510(k) clearances. Most are in product codes EBG (Crown And Bridge, Temporary, Resin) and EHP (Clasp, Preformed). 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 Inovativ, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Inovativ, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Inovativ, LLC by year, 2007–2026Sources: 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, Resin2decisions
  • EHPClasp, Preformed1decision

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.

  • K024282AcrylicInovativ, LLC · 20031cites it

What has FDA decided for it lately?

  • K024282AcrylicInovativ, LLC · 2003
  • K022032AcetalInovativ, LLC · 2002
  • K022030Poly-CarbInovativ, LLC · 2002

All 3 as Inovativ, LLC →