European Surgical, Inc.
Country not established
- Devices
- 1
What European Surgical, Inc. makes
European Surgical, Inc. manufactures endoscopic electrosurgical instruments and electrodes designed for minimally invasive surgical procedures, including tissue dissection, coagulation, and cutting.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does European Surgical, Inc. have in the registry?
The registry currently lists 1 device for European Surgical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list European Surgical, Inc.'s devices?
Among its 1 most recently registered device, European Surgical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do European Surgical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for European Surgical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from European Surgical, Inc. in the registry?
The most recently registered devices listed for European Surgical, Inc. include ENDOSCOPIC ELECTROSURGICAL INSTRUMENTS AND ELECTRODES.