Semperit Technische Produkte Gesellshaft is one of 21336 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Semperit Technische Produkte Gesellshaft - FDA 510(k) Cleared Devices
Recent clearances: SEMPERMED SUPREME, SIZES 5.5, 6, 6.5, 7, 7.5, 8, 8.5, AND 9, SEMPERMED DERMA PLUS, SIZES 5.5,6,6.5,7,7.5,8,8.5,9, SEMPERMED SURGEONS' GLOVES - SUPREME
3
Total
3
Cleared
0
Denied
Semperit Technische Produkte Gesellshaft has 3 FDA 510(k) cleared medical devices. Based in Apharetta, US.
Historical record: 3 cleared submissions from 1998 to 2002. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Semperit Technische Produkte Gesellshaft Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Semperit Technische Produkte Gesellshaft
3 devices