# Livetec GmbH

- Location (FDA's records): Loerrach, DE
- FDA decisions: 3 (2013–2015): 3 510(k) clearances
- Product codes: ILY (3)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K142722: 3B Laser 500, 3B Laser 200, LA-X P 500, LA-X P 200 (Jan 13, 2015)
- K142215: Power Twin21-50/Power Twin21-100 (Nov 7, 2014)
- K131797: 3B Laser Needle (Oct 10, 2013)

Source page: https://510kreport.com/company/livetec