510(k) Report

FDA applicant

Dentifax Intern, Inc.

York, PA1 decision1991–19910 recalls

FDA records 1 decision for Dentifax Intern, Inc. (York, PA) in 1991: 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 Dentifax Intern, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dentifax Intern, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dentifax Intern, 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?

  • 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.

  • K904251New Triad VLC Crown & Bridge Provisional MaterialDentifax Intern, Inc. · 19911cites it

What has FDA decided for it lately?

  • K904251New Triad VLC Crown & Bridge Provisional MaterialDentifax Intern, Inc. · 1991

The one decision as Dentifax Intern, Inc. →