510(k) Report

FDA applicant

Dental Vision Direct, Inc.

Los Angeles, CA2 decisions1994–19940 recalls

FDA records 2 decisions for Dental Vision Direct, Inc. (Los Angeles, CA) in 1994: 2 510(k) clearances. All are in product code EIA (Unit, Operative Dental). 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 Dental Vision Direct, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dental Vision Direct, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dental Vision Direct, Inc. 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?

  • EIAUnit, Operative Dental2decisions

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.

  • K933671UltracamDental Vision Direct, Inc. · 19942cite it
  • K941452Ultracam IIDental Vision Direct, Inc. · 19941cites it

What has FDA decided for it lately?

  • K941452Ultracam IIDental Vision Direct, Inc. · 1994
  • K933671UltracamDental Vision Direct, Inc. · 1994

All 2 as Dental Vision Direct, Inc. →