510(k) Report

FDA applicant

Dental Product Co.

Hammett, ID1 decision1990–19900 recalls

FDA records 1 decision for Dental Product Co. (Hammett, ID) in 1990: 1 510(k) clearance. All are in product code EBI (Resin, Denture, Relining, Repairing, Rebasing). 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 Product Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dental Product Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dental Product Co. 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?

  • EBIResin, Denture, Relining, Repairing, Rebasing1decision

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.

  • K901621New Per-Fit (R) ImprovedDental Product Co. · 19901cites it

What has FDA decided for it lately?

  • K901621New Per-Fit (R) ImprovedDental Product Co. · 1990

The one decision as Dental Product Co. →