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
1595465729
Device Listing 1595465729
Listing Summary
#
Listing key
1595465729
Premarket submission
K250597
Device
REMEX Xcam6
Applicant
Remedi, Inc.
Product code
IZL
Decision date
2025-07-31
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
229744
3013779985
3013779985
REMEDI INC.
1
N
2026-01-01
2F, 69-14, Sakju-ro 145beon-gil Chuncheon Gangwon KR 24232