Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1358759564
Device Listing 1358759564
Listing Summary
#
Listing key
1358759564
Premarket submission
K030147
Device
LUMENIS FAMILY OF ULTRAPULSE SURGITOUCH CO2 SURGICAL LASERS
Applicant
Lumenis, Ltd.
Product code
GEX
Decision date
2003-04-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
15660
3004135191
3004135191
LUMENIS, LTD.
1
N
2020-04-25
6 HAKIDMA STREET PO BOX 240 YOKNEAM INDUSTRIAL PARK YOKNEAM Ha Zafon IL 2069204