Weck Surgical Systems
Country not established
- Devices
- 1
What Weck Surgical Systems makes
Weck Surgical Systems manufactures a 25-watt carbon dioxide medical laser designed specifically for neurological surgical procedures.
This device is classified as Class III under FDA regulations and is 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 Weck Surgical Systems have in the registry?
The registry currently lists 1 device for Weck Surgical Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Weck Surgical Systems's devices?
Among its 1 most recently registered device, Weck Surgical Systems has devices listed in FDA 510(k) (1 device).
What risk classes do Weck Surgical Systems's devices fall under?
Among its 1 most recently registered device, the classes recorded for Weck Surgical Systems's devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Weck Surgical Systems in the registry?
The most recently registered devices listed for Weck Surgical Systems include 25 WATT CARBON DIOXIDE MEDICAL LASER FOR NEUROLOGY.