Lumenis

FDA Filings

This page includes the latest FDA filings for Lumenis. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Owner/Operator Registration

FDA Filings

Device Company	Device	Date
PMN K100415 LUMENIS	ACUPULSE 30/40 ST CO2 LASER SYSTEM AND ACUPULSE 40WG CO2 LASER SYSTEM	2010-04-21
PMN K030527 LUMENIS	LUMENIS FAMILY OF IPL AND COMBINATION IPL/ND:YAG SYSTEMS	2003-05-20
PMN K020591 LUMENIS	BCLEAR	2002-05-16
PMN K011197 LUMENIS	DERMACLEAR UV-B PHOTOTHERAPY SYSTEM	2001-12-14
PMA P990049S001 LUMENIS	COHERENT OPAL PHOTOACTIVATOR	2001-09-27
PMN K011703 LUMENIS	LUMENIS VERSAPULSE POWERSUITE HOLMIUM (HO:YAG) AND DUAL WAVELENGTH (HO:YAG/ND:YAG) SURGICAL LASERS AND DELIVERY DEVICES	2001-08-29
PMA P990049 LUMENIS	COHERENT OPAL PHOTOACTIVATOR LASER SYSTEM	2000-04-12

Similar & Related FDA Registered Companies

• LUMENIS, INC.
• LUMENIS LTD
• Lumenis Be, Inc.
• Lumenis Be, Ltd.