Topslane
Country not established
- Devices
- 1
What Topslane makes
Topslane develops the Anti-Tumor Expert System (ATES), a software-based tool designed for radiation therapy treatment planning. This system assists in optimizing tumor targeting and dose distribution during radiotherapy procedures, aiming to improve precision in cancer treatment.
The ATES is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States, where its device is authorized for use.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Topslane have in the registry?
The registry currently lists 1 device for Topslane. Devices recorded under merged duplicate company entries are counted once.
Which registries list Topslane's devices?
Among its 1 most recently registered device, Topslane has devices listed in FDA 510(k) (1 device).
What risk classes do Topslane's devices fall under?
Among its 1 most recently registered device, the classes recorded for Topslane's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Topslane in the registry?
The most recently registered devices listed for Topslane include ANTI-TUMOR EXPERT SYSTEM (ATES) FOR RADIATION THERAPY TREATMENT PLANNING.