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
2068762822
Device Listing 2068762822
Listing Summary
#
Listing key
2068762822
Premarket submission
K252246
Device
Leforte MMF System
Applicant
Jeil Medical Corporation
Product code
JEY
Decision date
2026-04-02
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