# Lxn Corp.

- Location (FDA's records): San Diego, CA
- FDA decisions: 7 (1996–2001): 7 510(k) clearances
- Product codes: CGA (5), LCP (1), JJX (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
- K002688: Personal Glucose Control Charting System (Feb 1, 2001)
- K991754: GO Glucose Monitoring System (Sep 8, 1999)
- K990942: Duet II Glucose Control Monitoring System (Aug 2, 1999)
- K973140: Duet Glucose Control Monitoring System (Oct 31, 1997)
- K962597: LXN Fructosamine Test System (Jun 13, 1997)
- K960034: LXN Blood Glucose Test System (Jun 28, 1996)
- K955629: LXN Fructosamine Test (Mar 20, 1996)

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