Biolase Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biolase Technology, Inc. - FDA 510(k) Cleared Devices
31
Total
31
Cleared
0
Denied
Biolase Technology, Inc. has 31 FDA 510(k) cleared general & plastic surgery devices. Based in Clemente, US.
Historical record: 31 cleared submissions from 1995 to 2013.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biolase Technology, Inc.
31 devices
Cleared
May 02, 2013
WATERLASE IPLUS ALL TISSUE LASER
General & Plastic Surgery
269d
Cleared
Apr 11, 2013
EPIC 10S
General & Plastic Surgery
45d
Cleared
Feb 01, 2013
DIOLASE 10S
General & Plastic Surgery
275d
Cleared
Sep 28, 2012
EPIC 10
General & Plastic Surgery
151d
Cleared
Aug 11, 2010
WATERLASE MD TURBO PLUS MODEL 7200XXX
General & Plastic Surgery
61d
Cleared
Mar 12, 2010
EZLASE 3 LASER SYSTEM
General & Plastic Surgery
86d
Cleared
Dec 07, 2009
WATERLASE MD, MODEL 7100102
General & Plastic Surgery
174d
Cleared
Oct 01, 2009
WATERLASE MD
General & Plastic Surgery
274d
Cleared
Jul 14, 2009
WATERLASE C100, MODEL 7100104
General & Plastic Surgery
14d
Cleared
Apr 14, 2009
EZLASE
Physical Medicine
130d
Cleared
Feb 11, 2009
WATERLASE MD
General & Plastic Surgery
16d
Cleared
Dec 22, 2008
EZLASE
General & Plastic Surgery
81d