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