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
1084775712
Device Listing 1084775712
Listing Summary
#
Listing key
1084775712
Premarket submission
K070570
Device
DIO IMPLANT SYSTEM
Applicant
Dio Department Dsi, Inc.
Product code
DZE
Decision date
2008-04-15
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
25196
3007126709
3007126709
DIO Corporation
1
N
2026-01-01
66, Centumseo-ro Haeundae-gu Busan KR 48058