Coalign Innovations, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Coalign Innovations, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Coalign Innovations, Inc. has 9 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 9 cleared submissions from 2011 to 2013. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Coalign Innovations, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Coalign Innovations, Inc.
9 devices
Cleared
Sep 12, 2013
ACCULIF TL AND PL CAGE
Orthopedic
31d
Cleared
Jun 19, 2013
COALIGN INNOVATIONS ACCULIF XL IBF CAGE
Orthopedic
30d
Cleared
Apr 03, 2013
ACCULIF XL CAGE
Orthopedic
65d
Cleared
Jan 23, 2013
ACCULIF TL-PEEK CAGE
Orthopedic
93d
Cleared
Jan 14, 2013
ACCULIF TL AND PL CAGE
Orthopedic
39d
Cleared
Jul 05, 2012
ACCULIF TL CAGE
Orthopedic
28d
Cleared
Dec 12, 2011
ACCULIF TL CAGE
Orthopedic
20d
Cleared
Dec 01, 2011
ACCULIF TL-PEEK IBF CAGE
Orthopedic
132d
Cleared
Apr 07, 2011
ACCULIF CAGE
Orthopedic
66d