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
1609637819
Device Listing 1609637819
Listing Summary
#
Listing key
1609637819
Premarket submission
K150161
Device
Venus Viva SR Device
Applicant
Venus Concept , Ltd.
Product code
GEI
Decision date
2015-05-12
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
128340
3008915316
3008915316
VENUS CONCEPT LTD.
1
N
2026-01-01
Hamelacha 1 St. Yokneam Illit Northern IL 2069812