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
1935183013
Device Listing 1935183013
Listing Summary
#
Listing key
1935183013
Premarket submission
K171285
Device
ARIX Diaphysis System
Applicant
Jeil Medical Corporation
Product code
HRS
Decision date
2017-07-24
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
21224
3004049923
3004049923
Priscilla Chung
1
N
2026-01-01
2552 Walnut Ave Ste 230 Tustin CA US 92780
223369
3014937101
3014937101
JEIL MEDICAL CORPORATION
1
N
2026-01-01
380, Beoman-ro Siheung-si Gyeonggi KR 14928