# Kronner Medical

- Location (FDA's records): Roseburg, OR
- FDA decisions: 7 (1987–1990): 7 510(k) clearances
- Product codes: KTT (3), LXH (1), JDW (1), HWT (1), CBT (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: 25 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K894228: Kronner Spherical Cutters (Jul 23, 1990)
- K895171: Blood Gas Safety Syringe (Nov 7, 1989)
- K895172: Kronner Sacral Pin Guide (Sep 12, 1989)
- K895173: Skeletal Fixation Pin (Sep 12, 1989)
- K871248: Kronner Colles-Forearm External Fixation (Jun 3, 1987)
- K871249: Kronner BI-Planer Tibia External Fixation (May 22, 1987)
- K871247: Kronner Universal Frame External Fixation (May 22, 1987)

Source page: https://510kreport.com/company/kronner-medical