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
1131021632
Device Listing 1131021632
Listing Summary
#
Listing key
1131021632
Premarket submission
K191123
Device
Multi-unit Abutments
Applicant
Medentika GmbH
Product code
NHA
Decision date
2020-01-06
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
123835
3008770646
3008770646
MEDENTIKA GMBH
1
N
2020-04-25
Hammweg 8-10 Huegelsheim Baden-Wurttemberg DE 76549
193864
3013232153
3013232153
Franz Menean
1
N
2020-04-25
112 CORPORATE DR Portsmouth NH US 03801