Syneron Beauty, Ltd.
Country not established
- Devices
- 4
What Syneron Beauty, Ltd. makes
Syneron Beauty manufactures non-invasive aesthetic devices, including systems designed for laser and intense pulsed light (IPL) treatments. These devices target skin rejuvenation, hair removal, and vascular lesion reduction through controlled energy delivery.
The company’s portfolio is regulated under Class II medical devices in the United States, with products authorised via the FDA’s 510(k) clearance process. These devices are listed in the FDA’s 510(k) database, adhering to regulatory standards for safety and performance.
Catalogue
Me Ref K131649
510(k) 510(k)Tanda Pearl, Ultrawyte, Pearl Ref K122725
510(k) 510(k)Tanda Mini Skincare System Ref K124042
510(k) 510(k)Me Ref K123845
510(k) 510(k)
Frequently asked questions
How many devices does Syneron Beauty, Ltd. have in the registry?
The registry currently lists 4 devices for Syneron Beauty, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Syneron Beauty, Ltd.'s devices?
Among its 4 most recently registered devices, Syneron Beauty, Ltd. has devices listed in FDA 510(k) (4 devices).
What risk classes do Syneron Beauty, Ltd.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Syneron Beauty, Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Syneron Beauty, Ltd. in the registry?
The most recently registered devices listed for Syneron Beauty, Ltd. include ME, TANDA PEARL, ULTRAWYTE, PEARL and TANDA MINI SKINCARE SYSTEM.