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
1855329357
Device Listing 1855329357
Listing Summary
#
Listing key
1855329357
Premarket submission
K053628
Device
LIGHTSHEER DUET LASER SYSTEM
Applicant
Lumenis, Inc.
Product code
GEX
Decision date
2006-04-07
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