Thermedical
Country not established
- Devices
- 1
What Thermedical makes
Thermedical manufactures the SERF Ablation System, including the SERF Ablation Needle, designed for tissue ablation procedures. These devices are intended for controlled removal or destruction of targeted tissue, commonly used in interventional radiology and oncology.
The SERF Ablation System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Serf Ablation System Serf Ablation Needle Ref K120116
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Thermedical have in the registry?
The registry currently lists 1 device for Thermedical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Thermedical's devices?
Among its 1 most recently registered device, Thermedical has devices listed in FDA 510(k) (1 device).
What risk classes do Thermedical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Thermedical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Thermedical in the registry?
The most recently registered devices listed for Thermedical include SERF ABLATION SYSTEM SERF ABLATION NEEDLE.