Sylphar N.V. is one of 118 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Sylphar N.V. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Sylphar N.V. has 2 FDA 510(k) cleared medical devices. Based in Rome, IT.
Historical record: 2 cleared submissions from 2013 to 2014. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Sylphar N.V. Filter by specialty or product code using the sidebar.
Sylphar N.V. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Feb 14, 2014
SYLPHAR REMESENSE SENSITIVITY RELIEF STRIPS
Dental
193d
Cleared
Jan 14, 2013
REMESENSE FOR SENSITIVE TEETH
Dental
132d