510(k) Report

FDA applicant

Diamodent

Anaheim, CA3 decisions2000–20040 recalls

FDA records 3 decisions for Diamodent (Anaheim, CA) from 2000 to 2004: 3 510(k) clearances. All are in product code DZE (Implant, Endosseous, Root-Form). 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 Diamodent’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Diamodent since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Diamodent 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?

  • DZEImplant, Endosseous, Root-Form3decisions

Who builds on its devices?

Later devices cite its devices 3 times; 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.

  • K993129Ucla/Universal AbutmentDiamodent · 20001cites it
  • K034022Ucla and Cement-on Abutments and AccessoriesDiamodent · 20041cites it
  • K010619Ucla and Universal AbutmentsDiamodent · 20011cites it

What has FDA decided for it lately?

  • K034022Ucla and Cement-on Abutments and AccessoriesDiamodent · 2004
  • K010619Ucla and Universal AbutmentsDiamodent · 2001
  • K993129Ucla/Universal AbutmentDiamodent · 2000

All 3 as Diamodent →