Palomar
Country not established
- Devices
- 2
What Palomar makes
Palomar makes the Palomar Dermalux Pulsed Light System and the Palomar LuxG Handpiece, which are light-based devices used for dermatological treatments.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Palomar Dermalux Pulsed Light System Ref K010618
Regimes: 510(k) Registry: 510(k)Palomar Luxg Handpiece Ref K020941
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Palomar have in the registry?
The registry currently lists 2 devices for Palomar. Devices recorded under merged duplicate company entries are counted once.
Which registries list Palomar's devices?
Among its 2 most recently registered devices, Palomar has devices listed in FDA 510(k) (2 devices).
What risk classes do Palomar's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Palomar's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Palomar in the registry?
The most recently registered devices listed for Palomar include PALOMAR DERMALUX PULSED LIGHT SYSTEM and PALOMAR LUXG HANDPIECE.