Lasercomp
Country not established
- Devices
- 2
What Lasercomp makes
Lasercomp manufactures diode laser systems, including the Model STAR 10, designed for surgical applications in oral, gynecology, and knee arthroscopy procedures. These devices are intended for precision tissue ablation, coagulation, and vaporization in controlled medical environments.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance for market authorisation. The devices are listed in the FDA’s 510(k) premarket notification database. Lasercomp operates with a US headquarters.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Lasercomp Model Star 10 For Knee Arthroscopy Ref K901127
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lasercomp have in the registry?
The registry currently lists 2 devices for Lasercomp. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lasercomp's devices?
Among its 2 most recently registered devices, Lasercomp has devices listed in FDA 510(k) (2 devices).
What risk classes do Lasercomp's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Lasercomp's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lasercomp in the registry?
The most recently registered devices listed for Lasercomp include LASERCOMP MODEL STAR 10 FOR ORAL, GYNECOLOGY SURG. and LASERCOMP MODEL STAR 10 FOR KNEE ARTHROSCOPY.