Surgicube International B.V.
NetherlandsFDA applicant, unverified
- Devices
- 1
What Surgicube International B.V. makes
Surgicube International B.V. manufactures the SurgiCube device, which is a Class II medical device.
The SurgiCube is listed in the FDA 510(k) registry, and the company is based in the US.
Catalogue
SurgiCube Ref K163455
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgicube International B.V. have in the registry?
The registry currently lists 1 device for Surgicube International B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgicube International B.V.'s devices?
Among its 1 most recently registered device, Surgicube International B.V. has devices listed in FDA 510(k) (1 device).
What risk classes do Surgicube International B.V.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Surgicube International B.V.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surgicube International B.V. in the registry?
The most recently registered devices listed for Surgicube International B.V. include SurgiCube.