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
1473046452
Device Listing 1473046452
Listing Summary
#
Listing key
1473046452
Premarket submission
K222482
Device
AGILON XO Shoulder System
Applicant
Implantcast GmbH
Product code
KWT
Decision date
2022-09-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
211185
3012523063
3012523063
Andrew Hewes
1
N
2026-01-01
13465 Midway Rd Ste 310 Dallas TX US 75244