Lasag AG
Country not established
- Devices
- 2
What Lasag AG makes
Lasag AG manufactures Q-switched Nd:YAG laser systems, including the Microruptor II for trabeculoplasty and the Microruptor III system, designed for ophthalmic procedures.
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
Lasag Microrupter 2 Nd:yag Laser Trabeculoplasty Ref K900199
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lasag AG have in the registry?
The registry currently lists 2 devices for Lasag AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lasag AG's devices?
Among its 2 most recently registered devices, Lasag AG has devices listed in FDA 510(k) (2 devices).
What risk classes do Lasag AG's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Lasag AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lasag AG in the registry?
The most recently registered devices listed for Lasag AG include LASAG MICRORUPTER 2 ND:YAG LASER TRABECULOPLASTY and MICRORUPTOR III SYST, Q-SWITCHED ND:YAG LASER COMP.