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
1606890369
Device Listing 1606890369
Listing Summary
#
Listing key
1606890369
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
164446
3004145084
3004145084
Bret Andre
1
N
2027-01-01
3762 Landis St West Linn OR US 97068