Kavo America is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kavo America - FDA 510(k) Cleared Devices
20
Total
19
Cleared
1
Denied
Kavo America has 19 FDA 510(k) cleared dental devices. Based in Washington, US.
Historical record: 19 cleared submissions from 1991 to 2008.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kavo America
20 devices
Cleared
Jul 10, 2008
KEY LASER III 1243 US WITH DETECT
General & Plastic Surgery
253d
Cleared
Oct 26, 2007
GENTLERAY 980 DIODE LASER SYSTEM
General & Plastic Surgery
72d
Cleared
Feb 08, 2007
KAVO EVEREST C-TEMP
Dental
64d
Cleared
Oct 21, 2005
DIAGNODENT
Dental
99d
Cleared
Aug 03, 2005
KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+
Dental
931d
Cleared
Jan 31, 2005
IN EXAM INTRAORAL DENTAL X-RAY SYSTEM
Radiology
26d
Cleared
Jul 24, 2003
KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60
Dental
17d
Cleared
Jul 09, 2003
PROPHYPEARLS
Dental
22d
Cleared
May 02, 2003
KAVO EVEREST G-BLANK, KAVO EVEREST G-CERAM, COATING CERAMIC LF-3-PFM, GLAZE...
Dental
65d
Cleared
Mar 12, 2003
KAVO EVEREST TITANBLANK
Dental
82d
Cleared
Jun 26, 2002
KAVO QUATTROCARE
Dental
338d
Cleared
Jan 14, 2002
KAVO POLYLUX II
Dental
84d