Livetec GmbH
Country not established
- Devices
- 3
What Livetec GmbH makes
Livetec GmbH manufactures laser-based medical devices, including the 3B Laser 500 and 200 series, LA-X P 500 and 200 series, and the 3B LASER NEEDLE for dermatological and cosmetic applications. The company also produces the Power Twin21-50 and Power Twin21-100, likely intended for tissue treatment or ablation procedures.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
3B Laser Needle Ref K131797
Regimes: 510(k) Registry: 510(k)Power Twin21-50/Power Twin21-100 Ref K142215
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Livetec GmbH have in the registry?
The registry currently lists 3 devices for Livetec GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Livetec GmbH's devices?
Among its 3 most recently registered devices, Livetec GmbH has devices listed in FDA 510(k) (3 devices).
What risk classes do Livetec GmbH's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Livetec GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Livetec GmbH in the registry?
The most recently registered devices listed for Livetec GmbH include 3B Laser 500, 3B Laser 200, LA-X P 500, LA-X P 200, 3B LASER NEEDLE and Power Twin21-50/Power Twin21-100.