# Ceramoptec GmbH

- Location (FDA's records): Bonn, DE
- FDA decisions: 2 (2021–2025): 2 510(k) clearances
- Product codes: GEX (2)
- Predicates its devices cite: 2 (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
- Olympus Surgical Technologies America: 1 (https://510kreport.com/company/olympus-surgical-technologies-america)
- A.R.C Laser GmbH: 1 (https://510kreport.com/company/arc-laser)

## Recent decisions
- K250504: Leonardo Duster (Jul 14, 2025)
- K210951: Leonardo Mini Blue (Sep 1, 2021)

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