Medical Device Manufacturer · US , Great Neck , NY

Mds - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2000

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Mds Dental ✕

1 devices

1-1 of 1

Cleared Jan 18, 2000

THE BI-DIRECTIONAL SPIRAL & EPOXY ROOT CANAL CEMENT SYSTEM