# Medifocus, Inc.

- Location (FDA's records): Columbia
- FDA decisions: 2 (1989–2004): 2 original PMA approvals
- Product codes: LNC (1), MEQ (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: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- P030006: Prolieve Thermodilatation  System (Feb 19, 2004)
- P880064: Hyperthermia System 100 a (Nov 17, 1989)

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