Ronvig A/S is one of 108 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Ronvig A/S - FDA 510(k) Cleared Devices
Recent clearances: B&R DEVICE, DENTO-PREP PARTICLE MICROBLASTER
2
Total
2
Cleared
0
Denied
Ronvig A/S has 2 FDA 510(k) cleared medical devices. Based in Dk-8721 Daugaard, DK.
Historical record: 2 cleared submissions from 2001 to 2003. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Ronvig A/S Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ronvig A/S
2 devices