Medical Device Manufacturer · US , Washington , DC

Kavo America - FDA 510(k) Cleared Devices

20 submissions · 19 cleared · Since 1991

Recent clearances: KEY LASER III 1243 US WITH DETECT, GENTLERAY 980 DIODE LASER SYSTEM, KAVO EVEREST C-TEMP

20

Total

19

Cleared

1

Denied

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

14 devices

1-12 of 14

Cleared Feb 08, 2007

KAVO EVEREST C-TEMP

Cleared Oct 21, 2005

Cleared Aug 03, 2005

KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+

Cleared Jul 24, 2003

KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60

Cleared Jul 09, 2003

Cleared May 02, 2003

KAVO EVEREST G-BLANK, KAVO EVEREST G-CERAM, COATING CERAMIC LF-3-PFM, GLAZE...

Cleared Mar 12, 2003

KAVO EVEREST TITANBLANK

Cleared Jun 26, 2002

KAVO QUATTROCARE

Cleared Jan 14, 2002

KAVO POLYLUX II

Cleared Nov 28, 2000

KAVO CORUND HANDPIECE 2013

Not Cleared Feb 22, 2000

KAVO DIAGNODENT

DEN990002 · NBL

Cleared Dec 19, 1997

PROPHYFLEX 2, MODEL 2012