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
1953206231
Device Listing 1953206231
Listing Summary
#
Listing key
1953206231
Premarket submission
K122493
Device
GENESISPLUS
Applicant
Cutera, Inc.
Product code
GEX
Decision date
2013-05-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
56563
2954354
3002900199
CUTERA, INC.
1
Y
2026-01-01
3240 BAYSHORE BLVD BRISBANE CA US 94005