# Nexus Medical, LLC

- Location (FDA's records): Lenexa, KS
- FDA decisions: 16 (2003–2015): 16 510(k) clearances
- Product codes: FPA (14), LJH (1), LHI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Kurin, Inc.: 1 (https://510kreport.com/company/kurin)

## Its most-cited devices
- K092382: Nexus Pressure Rated Extension Sets (2010), cited by 1

## Recent decisions
- K142590: All Safe Huber Safety Infusion Set (Jan 16, 2015)
- K133351: Nexus Nis-6P Luer Activated Device (May 22, 2014)
- K130879: Nexus IV Tubing Set with Luer-Accessbile One-Way Check Valve - IV Plus (Jul 9, 2013)
- K130416: Nexus Tko-6P Luer Activated Device (Jun 12, 2013)
- K113398: Nexus Tko-6, Luer-Activated Device (Apr 18, 2012)
- K092382: Nexus Pressure Rated Extension Sets (Apr 26, 2010)
- K092930: Nexus Intravascular Tubing Sets-Pre-Pierced (Mar 10, 2010)
- K092527: Nexus Injection Site, Model Nis-8 (Feb 4, 2010)

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