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
1858475612
Device Listing 1858475612
Listing Summary
#
Listing key
1858475612
Premarket submission
K140144
Device
BENDA WEDGE
Applicant
Centrix, Inc.
Product code
EJB
Decision date
2014-07-08
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
30768
1281412
1281412
CENTRIX, INC.
1
Y
2026-01-01
770 River Rd Shelton CT US 06484