Coherent Star
Country not established
- Devices
- 2
What Coherent Star makes
Coherent Star manufactures pulsed diode array laser systems, including the Lightsheer platform, designed for medical procedures requiring controlled tissue ablation or coagulation. These devices are intended for use in dermatology and aesthetic treatments, such as hair removal and skin resurfacing.
The company’s products fall under FDA Class II regulation and are authorised via the 510(k) clearance process. The portfolio is listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Lightsheer Pulsed Diode Array Laser System Ref K003614
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Coherent Star have in the registry?
The registry currently lists 2 devices for Coherent Star. Devices recorded under merged duplicate company entries are counted once.
Which registries list Coherent Star's devices?
Among its 2 most recently registered devices, Coherent Star has devices listed in FDA 510(k) (2 devices).
What risk classes do Coherent Star's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Coherent Star's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Coherent Star in the registry?
The most recently registered devices listed for Coherent Star include LIGHTSHEER PULSED DIODE ARRAY LASER SYSTEM and LIGHTSHEER PULSED DIODE ARRAY LASER SYSTEM (FAMILY OF PRODUCTS).