510(k) Report

FDA applicant

Novodent SA

Yverdons-Les-Bains, CH2 decisions2018–20200 recalls

FDA records 2 decisions for Novodent SA (Yverdons-Les-Bains, CH) from 2018 to 2020: 2 510(k) clearances. All are in product code DZE (Implant, Endosseous, Root-Form). Its devices cite 2 predicates, 1 of them its own earlier devices. 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 Novodent SA’s devices, and how often a recall has named them.

FDA decisions per year

1in 2020

2018: 12020: 1
2018high 1 (2018) · low 0 (2019)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2018.

FIG. 1 — Novodent SA by year, 2018–2026Sources: 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-Form2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 1 are its own earlier devices. The firms it cites most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K181266Implantswiss Dental Implant System, Implantswiss Dental Abutment SystemNovodent SA · 20181cites it

What has FDA decided for it lately?

  • K200867Implantswiss Dental Implant System and Implantswiss Dental Abutment SystemNovodent SA · 2020
  • K181266Implantswiss Dental Implant System, Implantswiss Dental Abutment SystemNovodent SA · 2018

All 2 as Novodent SA →