Chirurgie Innovation
FranceFDA 510(k) applicant, unverified
- Devices
- 21
What Chirurgie Innovation makes
Chirurgie Innovation manufactures plasma-based surgical electrodes and working elements for tissue resection and vaporization, including adaptors designed for integration with the Plasma Edge System. These devices are intended for use in minimally invasive procedures to remove or ablate tissue.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. The portfolio is listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Search and filter all 21 devicesCompany details
- DUNS number
- 264592326
Frequently asked questions
How many devices does CHIRURGIE INNOVATION have in the registry?
The registry currently lists 21 devices for CHIRURGIE INNOVATION. Devices recorded under merged duplicate company entries are counted once.
Which registries list CHIRURGIE INNOVATION's devices?
Among its 21 most recently registered devices, CHIRURGIE INNOVATION has devices listed in FDA 510(k) (2 devices) and FDA GUDID (19 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do CHIRURGIE INNOVATION's devices fall under?
Among its 21 most recently registered devices, the classes recorded for CHIRURGIE INNOVATION's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from CHIRURGIE INNOVATION in the registry?
The most recently registered devices listed for CHIRURGIE INNOVATION include Working element for FRONT load bipolar electrode Active working element ACMI compatible, Front load bipolar electrode, Working element for FRONT load bipolar electrode Passive working element STORZ compatible and Working element for FRONT load bipolar electrode Passive working element ACMI compatible.