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
1284468952
Device Listing 1284468952
Listing Summary
#
Listing key
1284468952
Premarket submission
K150064
Device
Synthetic Bone Graft (TriPore HA, TriPore BP90, TriPore BP15)
Applicant
Orthogem, Ltd.
Product code
MQV
Decision date
2015-09-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
72863
3006769747
3006769747
John Greenbaum
1
N
2020-04-25
3544 Amaca Cir Orlando FL US 32837