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
1388951451
Device Listing 1388951451
Listing Summary
#
Listing key
1388951451
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
323398
1644312
1000117748
MedXL
1
N
2026-01-01
3204 Hale Rd ARDMORE OK US 73401