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
1004552605
Device Listing 1004552605
Listing Summary
#
Listing key
1004552605
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
126610
1000122810
1000122810
Lumitex Medical Devices Inc.
1
N
2020-04-25
8300 Dow Circle Suite 400 Strongsville OH US 44136