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
1060929765
Device Listing 1060929765
Listing Summary
#
Listing key
1060929765
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
171229
3005533873
3005533873
Leeyeo Kee
1
N
2026-01-01
19 Holly Cove Ln. Dover DE US 19901