D3 Radiation Planning
Country not established
- Devices
- 1
What D3 Radiation Planning makes
D3 Radiation Planning develops a Commissioning Data Management System (CDMS), a software tool designed to organize, analyze, and document radiation treatment planning data for medical physics and oncology workflows. The system supports quality assurance processes by consolidating commissioning parameters, beam data, and calibration records in a structured format for clinical use.
The CDMS is classified as a Class II medical device under FDA regulations and requires 510(k) clearance for market authorization in the United States. The company is based in the US, and its device is listed in the FDA’s 510(k) database.
Catalogue
Commissioning Data Management System (Cdms) Ref K082606
510(k) 510(k)
Frequently asked questions
How many devices does D3 Radiation Planning have in the registry?
The registry currently lists 1 device for D3 Radiation Planning. Devices recorded under merged duplicate company entries are counted once.
Which registries list D3 Radiation Planning's devices?
Among its 1 most recently registered device, D3 Radiation Planning has devices listed in FDA 510(k) (1 device).
What risk classes do D3 Radiation Planning's devices fall under?
Among its 1 most recently registered device, the classes recorded for D3 Radiation Planning's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from D3 Radiation Planning in the registry?
The most recently registered devices listed for D3 Radiation Planning include COMMISSIONING DATA MANAGEMENT SYSTEM (CDMS).