510(k) Report

FDA applicant

Corinthian Medical, Ltd.

Amsterdam, NL1 decision2001–20010 recalls

FDA records 1 decision for Corinthian Medical, Ltd. (Amsterdam, NL) in 2001: 1 510(k) clearance. All are in product code NEA (Cement, Ear, Nose And Throat). 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 Corinthian Medical, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Corinthian Medical, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Corinthian Medical, Ltd. 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?

  • NEACement, Ear, Nose And Throat1decision

Who builds on its devices?

Later devices cite its devices 2 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.

  • K003567Serenocem, Model BC 010Corinthian Medical, Ltd. · 20012cite it

What has FDA decided for it lately?

  • K003567Serenocem, Model BC 010Corinthian Medical, Ltd. · 2001

The one decision as Corinthian Medical, Ltd. →