Osteogenics, Inc. is one of 7730 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Osteogenics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: STAR TEMPORARY WOUND COVER, BONESOURCE HYDROXYAPATITE CEMENT (HAC)
4
Total
4
Cleared
0
Denied
Osteogenics, Inc. has 4 FDA 510(k) cleared medical devices. Based in Burlington, US.
Historical record: 4 cleared submissions from 1996 to 2007. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Osteogenics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Osteogenics, Inc.
4 devices