Omnilife Science - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Omnilife Science has 7 FDA 510(k) cleared medical devices. Based in Raynham, US.
Last cleared in 2021. Active since 2007. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Omnilife Science Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Omnilife Science
7 devices
Cleared
Apr 02, 2021
Apex Knee System
Orthopedic
291d
Cleared
Dec 21, 2017
OMNI ARC Anteverted Neck Hip Stem
Orthopedic
128d
Cleared
Aug 17, 2017
OMNI Anseris Hip Stem
Orthopedic
119d
Cleared
Apr 26, 2017
Apex Revision Knee System
Orthopedic
149d
Cleared
Dec 21, 2015
Apex Revision Knee System
Orthopedic
24d
Cleared
Mar 13, 2014
OMNI ARC MONOBLOCK HIP STEM
Orthopedic
129d
Cleared
Aug 15, 2007
APEX HCLA ACETABULAR CUP LINERS
Orthopedic
355d