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
1831290463
Device Listing 1831290463
Listing Summary
#
Listing key
1831290463
Premarket submission
K261281
Device
CROSSLEAD Standard 035 and CROSSLEAD Stiff 035
Applicant
Filmecc Co., Ltd.
Product code
DQX
Decision date
2026-09-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
292262
3012223769
3008411636
FILMECC CO., LTD.
1
N
2026-01-01
3-99 Akatsuki-cho Seto-shi Aichi JP 4890071