Twinsight
FranceFDA 510(k) applicant, unverified
- Devices
- 1
What Twinsight makes
Twinsight manufactures the SurgiTwin, a surgical device designed for precise visualization and guidance during minimally invasive procedures.
The SurgiTwin is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
SurgiTwin Ref K250290
510(k) 510(k)
Frequently asked questions
How many devices does Twinsight have in the registry?
The registry currently lists 1 device for Twinsight. Devices recorded under merged duplicate company entries are counted once.
Which registries list Twinsight's devices?
Among its 1 most recently registered device, Twinsight has devices listed in FDA 510(k) (1 device).
What risk classes do Twinsight's devices fall under?
Among its 1 most recently registered device, the classes recorded for Twinsight's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Twinsight in the registry?
The most recently registered devices listed for Twinsight include SurgiTwin.