Medical Device Manufacturer · US , Reno , NV

Altatec GmbH - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 2006

Recent clearances: Altatec GmbH CAMLOG/CONELOG PROGRESSIVE-LINE Implants

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.

510(k) submissions have been managed by BioHorizons Implant Systems, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Altatec GmbH

14 devices
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