FDA applicant

Dmp Dental Industry S.A.

Markopoulo, GR3 decisions2020–20260 recalls

FDA records 3 decisions for Dmp Dental Industry S.A. (Markopoulo, GR) from 2020 to 2026: 3 510(k) clearances. Most are in product codes KLE (Agent, Tooth Bonding, Resin) and EJK (Liner, Cavity, Calcium Hydroxide). 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 Dmp Dental Industry S.A.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2020high 1 (2020) · low 0 (2021)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2020.

FIG. 1 — Dmp Dental Industry S.A. by year, 2020–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Dmp Dental Industry S.A.

Which product codes does it file in?

What has FDA decided for it lately?