510(k) Report

FDA applicant

Denar Corp.

Anaheim, CA5 decisions1985–19920 recalls

FDA records 5 decisions for Denar Corp. (Anaheim, CA) from 1985 to 1992: 5 510(k) clearances. Most are in product codes DZE (Implant, Endosseous, Root-Form) and IZT (Cone, Radiographic). 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 Denar Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Denar Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Denar Corp. 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
  • IZTCone, Radiographic1decision
  • IWYHolder, Head, Radiographic1decision

Who builds on its devices?

Later devices cite its devices 8 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.

  • K852802Denar Dental ImplantDenar Corp. · 19854cite it
  • K884845Steri-OssDenar Corp. · 19894cite it

What has FDA decided for it lately?

  • K925705Accurad-200 System & Accurad-300 Plus SystemDenar Corp. · 1992
  • K924759Collimator Light SourceDenar Corp. · 1992
  • K884845Steri-OssDenar Corp. · 1989
  • K883373Steri-Oss Hydroxyapatite-Coated Dental ImplantDenar Corp. · 1989
  • K852802Denar Dental ImplantDenar Corp. · 1985

All 5 as Denar Corp. →