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
1164854271
Device Listing 1164854271
Listing Summary
#
Listing key
1164854271
Premarket submission
K250809
Device
Stellar M22
Applicant
Lumenis Be, Ltd.
Product code
GEX
Decision date
2025-04-16
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
296730
3021349626
3021349626
Lumenis Be Ltd
1
N
2026-01-01
9 Hakidma St, POB # 426 Yokneam Industrial Park Yokneam, Ha Zafon 2069236 Haifa IL 2069236