Kavo America: 510(k) Clearances

24 510(k) clearances from Aug 26, 1991 to Jul 10, 2008, newest first. Showing 1 to 24.

What this list covers: FDA records filed under the name "Kavo America" and its spelling variant "Kavo America Corporation".

Back to the Kavo America profile

K-NumberDeviceDate
K073074KEY LASER III 1243 US WITH DETECTJul 10, 2008
K072262GENTLERAY 980 DIODE LASER SYSTEMOct 26, 2007
K063624KAVO EVEREST C-TEMPFeb 8, 2007
K051909DIAGNODENTOct 21, 2005
K030146KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+Aug 3, 2005
K042394DIAGNODENT PERIO TIP (ACCESSORY)Aug 2, 2005
K050744KAVO ERGOCOM/ERGOCAMApr 21, 2005
K050019IN EXAM INTRAORAL DENTAL X-RAY SYSTEMJan 31, 2005
K042872RONDOFLEX PLUS 360Nov 23, 2004
K033221KAVO EVEREST ZH-BLANKOct 28, 2003
K032081KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60Jul 24, 2003
K031868PROPHYPEARLSJul 9, 2003
K030607KAVO EVEREST G-BLANK, KAVO EVEREST G-CERAM, COATING CERAMIC LF-3-PFM, GLAZE AND…May 2, 2003
K024214KAVO EVEREST TITANBLANKMar 12, 2003
K012308KAVO QUATTROCAREJun 26, 2002
K013500KAVO POLYLUX IIJan 14, 2002
K002708KAVO CORUND HANDPIECE 2013Nov 28, 2000
K000805KAVO K.E.Y. LASER 1242May 4, 2000
DEN990002KAVO DIAGNODENTFeb 22, 2000
K983100KAVO KEY LASER 1242Jan 27, 1999
K973876PROPHYFLEX 2, MODEL 2012Dec 19, 1997
K940950KAVO SYSTEMATICA 1060Dec 29, 1994
K934783KAVO INTRASEPT 905May 16, 1994
K910789KAVOKLAVE STEAM AUTOCLAVEAug 26, 1991

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.