# Solitec GmbH

- Location (FDA's records): Planegg, DE
- FDA decisions: 3 (1983–1991): 3 510(k) clearances
- Product codes: IOB (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K903660: Dermalight Psoracomb (Jul 17, 1991)
- K828671: Uvatec Suntamed 4000 and 2000 (Jan 19, 1983)
- K828670: Uvatec Suntamed 400 (Jan 17, 1983)

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