Omni Life Science, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Omni Life Science, Inc. - FDA 510(k) Cleared Devices
Recent clearances: OMNI TiN Coated Apex Knee™ System
21
Total
21
Cleared
0
Denied
Omni Life Science, Inc. has 21 FDA 510(k) cleared orthopedic devices. Based in Raynham, US.
Historical record: 21 cleared submissions from 2006 to 2019.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Omni Life Science, Inc.
21 devices
Cleared
Sep 25, 2019
OMNI TiN Coated Apex Knee™ System
Orthopedic
86d
Cleared
Mar 10, 2016
OMNI Skirted Heads
Orthopedic
160d
Cleared
Oct 08, 2013
APEX KNEE MODULAR TIBIA SYSTEM
Orthopedic
139d
Cleared
Feb 29, 2012
APEX REVISION KNEE SYSTEMS
Orthopedic
152d
Cleared
Jan 05, 2012
APEX ARC HIP STEM
Orthopedic
64d
Cleared
Jul 13, 2011
APEX KNEE SYSTEM, APEX ALL POLY TIBIA
Orthopedic
86d
Cleared
Jun 27, 2011
APEX ARC HIP STEM
Orthopedic
60d
Cleared
Jun 22, 2011
APEX PS KNEE SYSTEM - PS-C INSERT
Orthopedic
56d
Cleared
Jun 16, 2011
APEX K1 HIP STEM
Orthopedic
73d
Cleared
Mar 25, 2011
APEX PS KNEE SYSTEM
Orthopedic
198d
Cleared
Sep 14, 2010
INTERFACE ACETABULAR SYSTEM, ACETABULAR INSERT +4 OFFSET
Orthopedic
63d
Cleared
Jun 22, 2010
APEX MODULE HIP SYSTEM BIOLOX DELTA FEMORAL HEAD
Orthopedic
28d