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
1085973737
Device Listing 1085973737
Listing Summary
#
Listing key
1085973737
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
106503
2087572
3000140642
EXPRESS MANUFACTURING, INC
1
N
2026-01-01
3519 West Warner Avenue Santa Ana CA US 92704