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
1868282668
Device Listing 1868282668
Listing Summary
#
Listing key
1868282668
Premarket submission
K090391
Device
PULPDENT MICRO-HYBRID COMPOSITE
Applicant
Pulpdent Corporation
Product code
EBF
Decision date
2009-05-11
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
29912
1215305
1215305
PULPDENT CORPORATION
1
Y
2026-01-01
80 Oakland St Watertown MA US 02472