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
1755963881
Device Listing 1755963881
Listing Summary
#
Listing key
1755963881
Premarket submission
K241445
Device
K-Bond Universal
Applicant
Spident Co., Ltd.
Product code
KLE
Decision date
2024-07-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
25225
3006113314
3006113314
SPIDENT CO., LTD.
1
N
2026-01-01
312, 151B-6L NAMDONGGONGDAN INCHEON Gyeonggi KR 405-821