# Dr. K. Honle GmbH

- Location (FDA's records): Walker, MI
- FDA decisions: 3 (1983–1983): 3 510(k) clearances
- 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
- K828675: Dermalight Uvastar 400 (Jan 17, 1983)
- K828674: Dermalight Blue-Point (Jan 17, 1983)
- K828676: Dermalight Spot (Jan 17, 1983)

Source page: https://510kreport.com/company/dr-k-honle