Adaptiiv is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Adaptiiv - FDA 510(k) Cleared Devices
Recent clearances: 3D Bolus Software Application, 3D Brachy Software Application, Patient-Matched 3D Printed Radiation Therapy Accessory
1
Total
1
Cleared
0
Denied
Adaptiiv has 1 FDA 510(k) cleared medical devices. Based in Halifax, CA.
Last cleared in 2022. Active since 2022. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Adaptiiv Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Adaptiiv
1 devices