Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled 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 13, 2026, FDA's public records list Altatec with 14 510(k) clearances. The most recent is a 510(k) clearance dated Sep 29, 2020: Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants.
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.
| Date | Record | Source |
|---|---|---|
| Sep 29, 2020 | Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE ImplantsK193401 · DZE | 510(k) clearances |
| Sep 14, 2016 | CAM Titanium BlanksK160784 · NHA | 510(k) clearances |
| Mar 31, 2016 | Abutment for BridgesK153779 · NHA | 510(k) clearances |
| Jan 12, 2016 | CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)K152509 · NHA | 510(k) clearances |
| Oct 2, 2015 | iSy Implant SystemK151599 · DZE | 510(k) clearances |
| Feb 17, 2015 | CONELOG Titanium base CAD/CAMK143337 · NHA | 510(k) clearances |
| Aug 6, 2014 | ISYK133991 · DZE | 510(k) clearances |
| Dec 14, 2012 | CONELOG IMPLANT SYSTEMK113779 · DZE | 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
