# Symbion, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 2 (1987–1988): 2 510(k) clearances
- Product codes: LDF (1), KFM (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
- K882129: Symbion Centrifugal Blood Pump Model I (Nov 3, 1988)
- K873474: Sutureless Temporary Epicardial Pacing Lead (Oct 7, 1987)

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