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
1714069368
Device Listing 1714069368
Listing Summary
#
Listing key
1714069368
Premarket submission
K041950
Device
APEX K2 HIP SYSTEM
Applicant
Apex Surgical, LLC
Product code
LPH
Decision date
2004-12-21
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