Inolase, Ltd.
Country not established
- Devices
- 1
What Inolase, Ltd. makes
Inolase, Ltd. makes the Candela-Inolase Serenity Pro PSF System, a laser-based device used for dermatological treatments.
The device is classified as Class II and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Candela-Inolase Serenity Pro Psf System Ref K072925
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Inolase, Ltd. have in the registry?
The registry currently lists 1 device for Inolase, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inolase, Ltd.'s devices?
Among its 1 most recently registered device, Inolase, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Inolase, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Inolase, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inolase, Ltd. in the registry?
The most recently registered devices listed for Inolase, Ltd. include CANDELA-INOLASE SERENITY PRO PSF SYSTEM.