Medical Device Manufacturer · US , Deer Field , IL

Kavo America Corporation - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2003

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Kavo America Corporation Dental ✕

3 devices

1-3 of 3

Cleared Aug 02, 2005

DIAGNODENT PERIO TIP (ACCESSORY)

Cleared Nov 23, 2004

RONDOFLEX PLUS 360

Cleared Oct 28, 2003

KAVO EVEREST ZH-BLANK