Syneron, Ltd.
IsraelFDA 510(k) applicant, unverified
- Devices
- 2
What Syneron, Ltd. makes
Syneron, Ltd. manufactures skin treatment systems, including the ETWO and EPLUS devices, which are designed for non-invasive cosmetic procedures such as hair removal, skin rejuvenation, and tattoo removal using advanced laser and light-based technologies.
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
Etwo Skin Treatment System Ref K110672
510(k) 510(k)Eplus Skin Treatment System Ref K113868
510(k) 510(k)
Frequently asked questions
How many devices does Syneron, Ltd. have in the registry?
The registry currently lists 2 devices for Syneron, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Syneron, Ltd.'s devices?
Among its 2 most recently registered devices, Syneron, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Syneron, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Syneron, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Syneron, Ltd. in the registry?
The most recently registered devices listed for Syneron, Ltd. include ETWO SKIN TREATMENT SYSTEM and EPLUS SKIN TREATMENT SYSTEM.