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
1506643089
Device Listing 1506643089
Listing Summary
#
Listing key
1506643089
Premarket submission
K875313
Device
PORCELAIN VENEER RESIN CEMENT W/DUAL CURE CATALYST
Applicant
Bisco, Inc.
Product code
EBF
Decision date
1988-03-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
80715
1420052
1420052
BISCO, INC.
1
N
2026-01-01
1100 WEST IRVING PARK RD. Schaumburg IL US 60193