Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Altatec GmbH

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories2
Latest FDA decision2020-09-29
TypeNumberDevice NameCodeDateActions
510(k) K193401 Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE ImplantsDZE2020-09-29 View
510(k) K160784 CAM Titanium BlanksNHA2016-09-14 View
510(k) K153779 Abutment for BridgesNHA2016-03-31 View
510(k) K152509 CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)NHA2016-01-12 View