Lumenis - FDA 510(k) Cleared Devices
Recent clearances: ACUPULSE 30/40 ST CO2 LASER SYSTEM AND ACUPULSE 40WG CO2 LASER SYSTEM, LUMENIS FAMILY OF IPL AND COMBINATION IPL/ND:YAG SYSTEMS, BCLEAR
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Lumenis General & Plastic Surgery ✕
5 devices
Cleared
Apr 21, 2010
ACUPULSE 30/40 ST CO2 LASER SYSTEM AND ACUPULSE 40WG CO2 LASER SYSTEM
General & Plastic Surgery
64d
Cleared
May 20, 2003
LUMENIS FAMILY OF IPL AND COMBINATION IPL/ND:YAG SYSTEMS
General & Plastic Surgery
90d
Cleared
May 16, 2002
BCLEAR
General & Plastic Surgery
83d
Cleared
Dec 14, 2001
DERMACLEAR UV-B PHOTOTHERAPY SYSTEM
General & Plastic Surgery
239d
Cleared
Aug 29, 2001
LUMENIS VERSAPULSE POWERSUITE HOLMIUM (HO:YAG) AND DUAL WAVELENGTH...
General & Plastic Surgery
89d