Medical Device Manufacturer · DK , Dk-8721 Daugaard

Ronvig A/S - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2001

Recent clearances: B&R DEVICE, DENTO-PREP PARTICLE MICROBLASTER

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Ronvig A/S Dental ✕

2 devices

1-2 of 2

Cleared Dec 22, 2003

Cleared May 10, 2001

DENTO-PREP PARTICLE MICROBLASTER

Data Source

Sourced from the FDA 510(k) public files . 176,583 total devices indexed.

Last updated: Oct 07, 2026