Temporaty Surgical Systems
Country not established
- Devices
- 1
What Temporaty Surgical Systems makes
Temporaty Surgical Systems manufactures the X-VEE device, which is categorized under Class II medical devices.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
X-Vee Ref K810152
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Temporaty Surgical Systems have in the registry?
The registry currently lists 1 device for Temporaty Surgical Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Temporaty Surgical Systems's devices?
Among its 1 most recently registered device, Temporaty Surgical Systems has devices listed in FDA 510(k) (1 device).
What risk classes do Temporaty Surgical Systems's devices fall under?
Among its 1 most recently registered device, the classes recorded for Temporaty Surgical Systems's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Temporaty Surgical Systems in the registry?
The most recently registered devices listed for Temporaty Surgical Systems include X-VEE.