Orthogem, Ltd. is one of 463 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Orthogem, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Synthetic Bone Graft (TriPore HA, TriPore BP90, TriPore BP15)
1
Total
1
Cleared
0
Denied
Orthogem, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Nottingham, GB.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Orthogem, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Priory Analysts, Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Orthogem, Ltd.
1 devices