Friandent GmbH is one of 25806 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Friandent GmbH - FDA 510(k) Cleared Devices
Recent clearances: MODIFICATION TO: XIVE 3.0 DENTAL IMPLANT SYSTEM, MULTIPLE, XIVE 3.0 DENTAL IMPLANT SYSTEM
2
Total
2
Cleared
0
Denied
Friandent GmbH has 2 FDA 510(k) cleared medical devices. Based in Lake Forest, US.
Historical record: 2 cleared submissions from 2003 to 2003. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Friandent GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Friandent GmbH
2 devices