Altatec GmbH is one of 12991 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Altatec GmbH - FDA 510(k) Cleared Devices
Recent clearances: Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants, CAM Titanium Blanks, Abutment for Bridges
14
Total
14
Cleared
0
Denied
Altatec GmbH has 14 FDA 510(k) cleared dental devices. Based in Reno, US.
Historical record: 14 cleared submissions from 2006 to 2020.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by PaxMed International, LLC and BioHorizons Implant Systems, Inc..
FDA 510(k) Regulatory Record - Altatec GmbH
14 devices
Cleared
Sep 29, 2020
Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants
Dental
298d
Cleared
Sep 14, 2016
CAM Titanium Blanks
Dental
176d
Cleared
Mar 31, 2016
Abutment for Bridges
Dental
91d
Cleared
Jan 12, 2016
CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)
Dental
132d
Cleared
Oct 02, 2015
iSy Implant System
Dental
112d
Cleared
Feb 17, 2015
CONELOG Titanium base CAD/CAM
Dental
89d
Cleared
Aug 06, 2014
ISY
Dental
223d
Cleared
Dec 14, 2012
CONELOG IMPLANT SYSTEM
Dental
358d
Cleared
Jan 10, 2011
CAMLOG VARIO SR ABUTMENTS
Dental
68d
Cleared
Jun 18, 2009
CAMLOG ABUTMENTS PS
Dental
127d
Cleared
Jan 30, 2009
CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS
Dental
66d
Cleared
Mar 05, 2008
CAMLOG IMPLANT SYSTEM ABUTMENTS
Dental
78d
Cleared
Aug 10, 2007
CAMLOG LOGFIT PROSTHETIC SYSTEM
Dental
101d
Cleared
Feb 17, 2006
CAMLOG DENTAL IMPLANT ABUTMENTS, HEALING CAPS, AND ACCESSORIES
Dental
242d