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
2041721642
Device Listing 2041721642
Listing Summary
#
Listing key
2041721642
Premarket submission
K222738
Device
Point implant system
Applicant
Pointnix Co., Ltd.
Product code
DZE
Decision date
2023-04-13
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
298236
3011891801
3011891801
Dave Kim
1
N
2026-01-01
7505 Fannin St Ste 610 Houston TX US 77054