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
1349959337
Device Listing 1349959337
Listing Summary
#
Listing key
1349959337
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
105348
3007708502
3007708502
Filippo Bastia
1
N
2026-01-01
1731 SE Oralabor Road Ankeny IA US 50021