Dr. Ihde Dental AG Switzerland is one of 10620 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dr. Ihde Dental AG Switzerland - FDA 510(k) Cleared Devices
Recent clearances: ALLFIT IMPLANT SYSTEM, SHORT NECK, MODEL STI RT LENGTH, ALLFIT IMPLANT SYSTEM, LONG NECK, MODEL STI RT LN LENGTH
1
Total
1
Cleared
0
Denied
Dr. Ihde Dental AG Switzerland has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Dr. Ihde Dental AG Switzerland Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dr. Ihde Dental AG Switzerland
1 devices