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
1075956080
Device Listing 1075956080
Listing Summary
#
Listing key
1075956080
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
20580
3003741796
3003741796
Leeyeo Kee
1
N
2026-01-01
19 Holly Cove Ln. Suite 200 Dover DE US 19901