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
1324072117
Device Listing 1324072117
Listing Summary
#
Listing key
1324072117
Premarket submission
K221342
Device
REDEMPTION Beaming System
Applicant
Vilex, LLC
Product code
HWC
Decision date
2022-12-13
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
29296
1051526
1051526
Vilex LLC
1
Y
2026-01-01
111 MOFFITT ST MCMINNVILLE TN US 37110