Laserscope
Country not established
- Devices
- 60
What Laserscope makes
Laserscope manufactures surgical laser systems and associated accessories for precision tissue treatment, including Nd:YAG, Er:YAG, and KTP laser platforms. Products include systems for ophthalmic, neurosurgical, and otolaryngological procedures, as well as micromanipulators and delivery devices for controlled energy application. The portfolio also covers photodynamic and photocoagulation therapies, with configurations for both continuous-wave and Q-switched operation.
All listed devices fall under Class II regulatory classification in the US, with authorisation via 510(k) premarket notifications through the FDA. The company’s products are registered under the FDA 510(k) database, and the manufacturer is based in the United States.
Catalogue
Search and filter all 60 devicesShowing 1-50 of 60
Frequently asked questions
How many devices does Laserscope have in the registry?
The registry currently lists 60 devices for Laserscope. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laserscope's devices?
Among its 50 most recently registered devices, Laserscope has devices listed in FDA 510(k) (50 devices).
What risk classes do Laserscope's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Laserscope's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Laserscope in the registry?
The most recently registered devices listed for Laserscope include KTP/532 & KTP/YAG, KTP/YAG AND KTP/YAG PLUS, KTP/532 AND KTP/YAG and KTP/532 LASER.