Laser Surgical Systems
Country not established
- Devices
- 2
What Laser Surgical Systems makes
Laser Surgical Systems manufactures disposable active electrodes, such as the SUREPEN™, and fiber-based medical devices like FIBERLIFE, designed for surgical and laser applications.
These products fall under FDA Class II regulation and are listed via 510(k) clearance. The company operates from the United States.
Catalogue
Surepen(Tm) Disposable Active Electrodes Ref K925266
Regimes: 510(k) Registry: 510(k)Fiberlife Ref K922807
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Laser Surgical Systems have in the registry?
The registry currently lists 2 devices for Laser Surgical Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laser Surgical Systems's devices?
Among its 2 most recently registered devices, Laser Surgical Systems has devices listed in FDA 510(k) (2 devices).
What risk classes do Laser Surgical Systems's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Laser Surgical Systems's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Laser Surgical Systems in the registry?
The most recently registered devices listed for Laser Surgical Systems include SUREPEN(TM) DISPOSABLE ACTIVE ELECTRODES and FIBERLIFE.