Altatec GmbH

Altatec GmbH holds 14 FDA 510(k) medical device clearances, first cleared 2006, most recent 2020.

Top product codes for Altatec GmbH

NHA — Dental9 devices
DZE — Dental5 devices

Recent clearances by Altatec GmbH

K193401 — Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE ImplantsCode DZE·2020-09-29
K160784 — CAM Titanium BlanksCode NHA·2016-09-14
K153779 — Abutment for BridgesCode NHA·2016-03-31
K152509 — CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)Code NHA·2016-01-12
K151599 — iSy Implant SystemCode DZE·2015-10-02
K143337 — CONELOG Titanium base CAD/CAMCode NHA·2015-02-17
K133991 — ISYCode DZE·2014-08-06
K113779 — CONELOG IMPLANT SYSTEMCode DZE·2012-12-14
K103252 — CAMLOG VARIO SR ABUTMENTSCode NHA·2011-01-10
K090347 — CAMLOG ABUTMENTS PSCode NHA·2009-06-18
K083496 — CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTSCode DZE·2009-01-30
K073553 — CAMLOG IMPLANT SYSTEM ABUTMENTSCode NHA·2008-03-05
K071213 — CAMLOG LOGFIT PROSTHETIC SYSTEMCode NHA·2007-08-10
K051636 — CAMLOG DENTAL IMPLANT ABUTMENTS, HEALING CAPS, AND ACCESSORIESCode NHA·2006-02-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.