Wavelight Laser Technologie AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Wavelight Laser Technologie AG - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Wavelight Laser Technologie AG has 8 FDA 510(k) cleared medical devices. Based in North Reading, US.
Historical record: 8 cleared submissions from 2004 to 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Wavelight Laser Technologie AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Wavelight Laser Technologie AG
8 devices
Cleared
Feb 22, 2006
WAVELIGHT IDAS
General & Plastic Surgery
57d
Cleared
Oct 17, 2005
BURANE
General & Plastic Surgery
13d
Cleared
Jun 30, 2005
WAVELIGHT AURIGA
General & Plastic Surgery
30d
Cleared
Feb 24, 2005
BURANE XL
General & Plastic Surgery
15d
Cleared
Feb 15, 2005
WAVELIGHT SINON
General & Plastic Surgery
15d
Cleared
Sep 29, 2004
ARION
General & Plastic Surgery
16d
Cleared
May 19, 2004
SINON
General & Plastic Surgery
90d
Cleared
May 14, 2004
MYDON C
General & Plastic Surgery
87d