# Orangedental GmbH & Co. KG

- Location (FDA's records): Biberach, DE
- FDA decisions: 1 (2007–2007): 1 510(k) clearance
- Product codes: LLZ (1)
- Predicates its devices cite: 1 (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

## Firms whose devices it cites most
- Apteryx, Inc.: 1 (https://510kreport.com/company/apteryx)

## Recent decisions
- K072665: Suniray 5.2 (Oct 3, 2007)

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