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
1432350265
Device Listing 1432350265
Listing Summary
#
Listing key
1432350265
Premarket submission
K232405
Device
ENDOFIX EXO
Applicant
Aktormed GmbH
Product code
OCV
Decision date
2024-04-25
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
226832
3011390076
3011390076
AKTORmed GmbH
1
N
2026-01-01
Neugablonzer Strasse 13 Neutraubling Bavaria DE 93073