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
1394463579
Device Listing 1394463579
Listing Summary
#
Listing key
1394463579
Premarket submission
K875133
Device
CAVIT-W
Applicant
Espe GmbH (Us)
Product code
EBG
Decision date
1988-03-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
350787
3045891668
3045891668
FRONTIER DENTAL SUPPLY INC
1
N
2027-01-01
450 Addison Hall Circle, Unit 9-12 Aurora Ontario CA L4G 7C7