Medical Device Manufacturer · US , Lake Forest , CA

Friandent GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2003

Recent clearances: MODIFICATION TO: XIVE 3.0 DENTAL IMPLANT SYSTEM, MULTIPLE, XIVE 3.0 DENTAL IMPLANT SYSTEM

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Friandent GmbH Dental ✕

2 devices

1-2 of 2

Cleared Oct 02, 2003

MODIFICATION TO: XIVE 3.0 DENTAL IMPLANT SYSTEM, MULTIPLE

Cleared Aug 12, 2003

XIVE 3.0 DENTAL IMPLANT SYSTEM