Endocure Technologies, Inc.
Country not established
- Devices
- 1
What Endocure Technologies, Inc. makes
Endocure Technologies, Inc. manufactures the EndoCure Model EUR078A, a medical device designed for localized tumor ablation using radiofrequency energy, intended for use in oncological procedures.
The company’s portfolio is regulated under FDA’s Class II device classification and is listed via 510(k) clearance. The device is based in the United States.
Catalogue
EndoCure Model EUR078A Ref K161147
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endocure Technologies, Inc. have in the registry?
The registry currently lists 1 device for Endocure Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endocure Technologies, Inc.'s devices?
Among its 1 most recently registered device, Endocure Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Endocure Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Endocure Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endocure Technologies, Inc. in the registry?
The most recently registered devices listed for Endocure Technologies, Inc. include EndoCure Model EUR078A.