Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ItalyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Mectron S.p.A. with 13 510(k) clearances. The most recent is a 510(k) clearance dated May 9, 2025: turbodent touch.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| May 9, 2025 | turbodent touchK251425 · KOJ | 510(k) clearances |
| Aug 19, 2024 | MT-BoneK242432 · DZI | 510(k) clearances |
| May 15, 2023 | Combi TouchK231391 · ELC | 510(k) clearances |
| Apr 13, 2018 | Piezosurgery WhiteK171326 · DZI | 510(k) clearances |
| Jan 12, 2018 | PIEZOSURGERY TOUCH, PIEZOSURGERY WHITEK171958 · DZI | 510(k) clearances |
| May 25, 2016 | PIEZOSURGERY PLUSK153743 · JDX | 510(k) clearances |
| Sep 4, 2015 | PIEZOSURGERY WHITEK151248 · DZI | 510(k) clearances |
| Aug 5, 2015 | COMPACT PIEZO LEDK151023 · ELC | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
