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
1995387321
Device Listing 1995387321
Listing Summary
#
Listing key
1995387321
Premarket submission
K113242
Device
APEX ARC HIP STEM
Applicant
Omni Life Science, Inc.
Product code
LPH
Decision date
2012-01-05
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
346796
1226188
3008342029
OMNIlifeScience, Inc.
1
Y
2026-01-01
480 Paramount Dr Raynham MA US 02767