# Ecleris USA

- Location (FDA's records): San Diego, CA
- FDA decisions: 2 (2010–2014): 2 510(k) clearances
- Product codes: HEX (1), EOB (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: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K131323: Ecleris Sinuscope (Jun 9, 2014)
- K100595: Ecleris Microstar Colposcope (Jul 9, 2010)

Source page: https://510kreport.com/company/ecleris-usa