Precise Light Surgical
Country not established
- Devices
- 1
What Precise Light Surgical makes
Precise Light Surgical manufactures O-pel Laser systems and associated probe delivery devices designed for surgical applications, including precision tissue ablation and coagulation.
These devices are classified as Class II under FDA regulations and are 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 Precise Light Surgical have in the registry?
The registry currently lists 1 device for Precise Light Surgical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Precise Light Surgical's devices?
Among its 1 most recently registered device, Precise Light Surgical has devices listed in FDA 510(k) (1 device).
What risk classes do Precise Light Surgical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Precise Light Surgical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Precise Light Surgical in the registry?
The most recently registered devices listed for Precise Light Surgical include O-pel Laser and families of probe delivery devices.