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
1382092082
Device Listing 1382092082
Listing Summary
#
Listing key
1382092082
Premarket submission
K191890
Device
Elos Accurate Customized Abutment
Applicant
Elos Medtech Pinol A/S
Product code
NHA
Decision date
2020-02-06
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
102756
3007689689
3007689689
ELOS MEDTECH PINOL A/S
1
N
2026-01-01
Engvej 33 Goerloese Hovedstaden DK DK3330