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
2054205040
Device Listing 2054205040
Listing Summary
#
Listing key
2054205040
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
178155
1954435
3003110749
ESCREEN, INC.
1
N
2020-04-25
8140 Ward Parkway Suite 300 Kansas City MO US 64114
177997
2032598
3003789989
AMEDITECH, INC.
1
N
2020-04-25
9940 Mesa Rim Rd SAN DIEGO CA US 92121