Zygofix , Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Zygofix , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Misgav, IL.
Latest FDA clearance: Sep 2024. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Zygofix , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
2 devices