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
1198752116
Device Listing 1198752116
Listing Summary
#
Listing key
1198752116
Premarket submission
K242703
Device
LW Pre-milled Abutment
Applicant
Ossvis Co., Ltd.
Product code
NHA
Decision date
2024-12-05
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
310429
3025338240
3025338240
OSSVIS CO., LTD.
1
N
2026-01-01
6F, 7F and B1, 38, Burim-ro 170beon-gil, Dongan-gu Anyang-si Gyeonggi KR 14055