# Kyocera International, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 3 (1976–1986): 3 510(k) clearances
- Product codes: DZE (2), EIH (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
- K860360: Kyocera Bioceram Porous Dental Implant (Apr 4, 1986)
- K854763: Cerapearl (Feb 21, 1986)
- K760008: Dental Material, Implant, High-Purity AL (Oct 5, 1976)

Source page: https://510kreport.com/company/kyocera-international
