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
1345039215
Device Listing 1345039215
Listing Summary
#
Listing key
1345039215
Premarket submission
K111193
Device
APEX ARC HIP STEM
Applicant
Omni Life Science, Inc.
Product code
LZO
Decision date
2011-06-27
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
56297
1226188
3008342029
OMNIlifeScience, Inc.
1
Y
2020-04-25
480 Paramount Dr Raynham MA US 02767