Osseofuse, Inc. is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Osseofuse, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Osseofuse, Inc. has 2 FDA 510(k) cleared medical devices. Based in Brea, US.
Historical record: 2 cleared submissions from 2013 to 2014. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Osseofuse, Inc. Filter by specialty or product code using the sidebar.
Osseofuse, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Sep 19, 2014
ONE PLUS IMPLANT SYSTEM
Dental
357d
Cleared
Oct 31, 2013
OSSEOFUSE DENTAL IMPLANT SYSTEM
Dental
139d