Dormotech Medical, Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Dormotech Medical, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Afula, IL.
Latest FDA clearance: Jan 2025. Active since 2023. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Dormotech Medical, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by ProMedic Consulting, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
2 devices