Adaptiiv
CanadaFDA applicant, unverified
- Devices
- 1
What Adaptiiv makes
Adaptiiv develops software applications and patient-matched 3D printed accessories for radiation therapy. Their 3D Bolus Software Application and 3D Brachy Software Application assist in treatment planning and customisation. The company also produces 3D printed radiation therapy accessories tailored to individual patients.
These products are classified as Class II medical devices under FDA regulations and are authorised via the 510(k) pathway. Adaptiiv is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Adaptiiv have in the registry?
The registry currently lists 1 device for Adaptiiv. Devices recorded under merged duplicate company entries are counted once.
Which registries list Adaptiiv's devices?
Among its 1 most recently registered device, Adaptiiv has devices listed in FDA 510(k) (1 device).
What risk classes do Adaptiiv's devices fall under?
Among its 1 most recently registered device, the classes recorded for Adaptiiv's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Adaptiiv in the registry?
The most recently registered devices listed for Adaptiiv include 3D Bolus Software Application, 3D Brachy Software Application, Patient-Matched 3D Printed Radiation Therapy Accessory.