# Veridex, LLC

- Location (FDA's records): Raritan, NJ
- FDA decisions: 12 (2004–2013): 12 510(k) clearances
- Product codes: NQI (10), GKH (1), NRS (1)
- Predicates its devices cite: 10 (6 its own); citations of its devices by later devices: 6 (6 its own)
- Recalls linked to its devices: 10 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Immunicon Corp.: 2 (https://510kreport.com/company/immunicon)
- Advanced Diagnostic Systems: 2 (https://510kreport.com/company/advanced-diagnostic-systems)

## Its most-cited devices
- K110406: Celltracks Autoprep System (2012), cited by 1
- K071729: Cellsearch Circulating Tumor Cell Kit (2007), cited by 1
- K073338: Cellsearch Circulating Tumor Cell Kit (2008), cited by 1
- K050245: Cellsearch Circulating Tumor Cell Kit (2005), cited by 1
- K113181: Celltracks Analyer II (2011), cited by 1
- K062013: Cellsearch Circulating Tumor Cell Kit (2006), cited by 1

## Recent decisions
- K130794: Celltracks Analyzer II System (Jun 20, 2013)
- K122821: Celltracks Autoprep System (Dec 13, 2012)
- K110406: Celltracks Autoprep System (Jan 20, 2012)
- K113181: Celltracks Analyer II (Dec 12, 2011)
- K103502: Cellsearch Circulating Tumor Cell Kit Model 7900001 (Dec 21, 2010)
- K100684: Celltracks Autoprep System Model:9541 (Aug 26, 2010)
- K073338: Cellsearch Circulating Tumor Cell Kit (Feb 26, 2008)
- K071729: Cellsearch Circulating Tumor Cell Kit (Nov 20, 2007)

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