Medical Device Manufacturer · IT , Rome

Sylphar N.V. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2013

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Sylphar N.V. Dental ✕

2 devices

1-2 of 2

Cleared Feb 14, 2014

SYLPHAR REMESENSE SENSITIVITY RELIEF STRIPS

Cleared Jan 14, 2013

REMESENSE FOR SENSITIVE TEETH