Orthospin, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Orthospin, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: AutoStrut G2
1
Total
1
Cleared
0
Denied
Orthospin, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Yokneam, IL.
Last cleared in 2021. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Orthospin, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Orthospin, Ltd.
1 devices