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FDA 510(k) Applications Submitted by KAVO AMERICA
FDA 510(k) Number
Submission Date
Device Name
Applicant
K031868
06/17/2003
PROPHYPEARLS
KAVO AMERICA
K032081
07/07/2003
KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60
KAVO AMERICA
K073074
10/31/2007
KEY LASER III 1243 US WITH DETECT
KAVO AMERICA
K063624
12/06/2006
KAVO EVEREST C-TEMP
KAVO AMERICA
K051909
07/14/2005
DIAGNODENT
KAVO AMERICA
DEN990002
07/12/1999
KAVO DIAGNODENT
KAVO AMERICA
K983100
09/03/1998
KAVO KEY LASER 1242
KAVO AMERICA
K973876
10/10/1997
PROPHYFLEX 2, MODEL 2012
KAVO AMERICA
K030146
01/15/2003
KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+
KAVO AMERICA
K030607
02/26/2003
KAVO EVEREST G-BLANK, KAVO EVEREST G-CERAM, COATING CERAMIC LF-3-PFM, GLAZE AND COLORINGS/STAINING/SHADES
KAVO AMERICA
K013500
10/22/2001
KAVO POLYLUX II
KAVO AMERICA
K000805
03/13/2000
KAVO K.E.Y. LASER 1242
KAVO AMERICA
K072262
08/15/2007
GENTLERAY 980 DIODE LASER SYSTEM
KAVO AMERICA
K012308
07/23/2001
KAVO QUATTROCARE
KAVO AMERICA
K002708
08/30/2000
KAVO CORUND HANDPIECE 2013
KAVO AMERICA
K024214
12/20/2002
KAVO EVEREST TITANBLANK
KAVO AMERICA
K050019
01/05/2005
IN EXAM INTRAORAL DENTAL X-RAY SYSTEM
KAVO AMERICA
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