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
1021468648
Device Listing 1021468648
Listing Summary
#
Listing key
1021468648
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
165008
3005952241
3005952241
Leeyeo Kee
1
N
2026-01-01
19 Holly Cove Ln., Dover DE US 19901