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
1505646761
Device Listing 1505646761
Listing Summary
#
Listing key
1505646761
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
78556
3004101653
3004101653
Wendy Ko
1
N
2026-01-01
1511 S. Carlos Avenue Ontario CA US 91761