Orthocrat, Ltd. is one of 503 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Orthocrat, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: TRAUMACAD VERSION 2.0, TRAUMACAD 1.2
2
Total
2
Cleared
0
Denied
Orthocrat, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Tel Aviv, IL.
Historical record: 2 cleared submissions from 2004 to 2008. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Orthocrat, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Citech as regulatory consultant.
FDA 510(k) Regulatory Record - Orthocrat, Ltd.
2 devices