Dornier Medtech America, Inc. - FDA 510(k) Cleared Devices
40
Total
40
Cleared
0
Denied
FDA 510(k) cleared devices by Dornier Medtech America, Inc. General & Plastic Surgery ✕
23 devices
Cleared
Jul 28, 2016
Medilas H Laser Fibers
General & Plastic Surgery
30d
Cleared
Oct 08, 2015
Medilas H RFID Laser Fibers
General & Plastic Surgery
28d
Cleared
Mar 21, 2013
DORNIER MEDILAS UROPULSE
General & Plastic Surgery
38d
Cleared
Feb 01, 2013
DORNIER MEDILAS H30 SOLVO
General & Plastic Surgery
196d
Cleared
Dec 14, 2012
MEDILAS H LASER FIBERS
General & Plastic Surgery
42d
Cleared
Aug 01, 2012
MEDILAS H RFID LASER FIBER
General & Plastic Surgery
30d
Cleared
Dec 07, 2011
DORNIER MEDILAS D LITEBEAM+ 1470
General & Plastic Surgery
303d
Cleared
Feb 12, 2009
MEDILAS D FAMILY LASERS, INCLUDING MEDILAS D LITEBEAM, LITEBEAM +, UROBEAM,...
General & Plastic Surgery
79d
Cleared
Jan 30, 2009
MEDILAS D FAMILY LASERS, INCLUDING MEDILAS D LITEBEAM, LITEBEAM +, UROBEAM,...
General & Plastic Surgery
87d
Cleared
Aug 20, 2008
MEDILAS D FAMILY LASERS
General & Plastic Surgery
258d
Cleared
Jun 27, 2008
DORNIER MEDILAS D 30 LASER, MEDILAS D 1064
General & Plastic Surgery
85d
Cleared
May 21, 2007
MEDILAS D FAMILY LASERS
General & Plastic Surgery
84d