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
1069632849
Device Listing 1069632849
Listing Summary
#
Listing key
1069632849
Premarket submission
K961511
Device
HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER
Applicant
Lifecore Biomedical, Inc.
Product code
LZK
Decision date
1996-06-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
223727
3003845138
3003845138
Keystone Dental Inc.
1
N
2020-04-25
5 Holland Building 209 Irvine CA US 92618