Diagnostics makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Johnson & JohnsonLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record. See the Johnson & Johnson group view.
As of Nov 13, 2026, FDA's public records list Veridex, LLC with 12 510(k) clearances and 4 device recalls. The most recent is a device recall dated May 15, 2015: Cell Search Circulating Tumor Kit. Intended for the enumeration of circulating tumor cel….
| Date | Record | Source |
|---|---|---|
| May 15, 2015 | Cell Search Circulating Tumor Kit. Intended for the enumeration of circulating tumor cells (CTC) of epithelial origin in whole blood.Class II · Complaints of the presence of artifacts that appears as small bead like structures in the image gallery when processing | Device recalls |
| Jan 8, 2014 | CELLTRACKS ANALYZER II¿ (Product Code 9555) Product Usage: The CELLTRACKS ANALYZER II¿ is a semi-automated fluorescence microscope, coClass II · Janssen Diagnostics, LLC received complaints of camera failures on the CELLTRACKS ANALYZER II¿. | Device recalls |
| Jun 20, 2013 | CELLTRACKS ANALYZER II SYSTEMK130794 · NQI | 510(k) clearances |
| Dec 28, 2012 | CELLTRACKS AUTOPREP System (Software Version 2.4.1 & Below. Product Usage: The CELLTRACKS AUTOPREP System is a general purpose laboratClass II · Veridex, LLC has received a report that a patient's demographics were incorrectly associated with another patient's iden | Device recalls |
| Dec 28, 2012 | CELLTRACKS ANALYZER II (Software Version 2.5.1 & Below. Product Usage: The CELLTRACKS AUTOPREP System is a general purpose laboratory Class II · Veridex, LLC has received a report that a patient's demographics were incorrectly associated with another patient's iden | Device recalls |
| Dec 13, 2012 | CELLTRACKS AUTOPREP SYSTEMK122821 · NQI | 510(k) clearances |
| Jan 20, 2012 | CELLTRACKS AUTOPREP SYSTEMK110406 · NQI | 510(k) clearances |
| Dec 12, 2011 | CELLTRACKS ANALYER IIK113181 · NQI | 510(k) clearances |
| Dec 21, 2010 | CELLSEARCH CIRCULATING TUMOR CELL KIT MODEL 7900001K103502 · NQI | 510(k) clearances |
| Aug 26, 2010 | CELLTRACKS AUTOPREP SYSTEM MODEL:9541K100684 · GKH | 510(k) clearances |
| Feb 26, 2008 | CELLSEARCH CIRCULATING TUMOR CELL KITK073338 · NQI | 510(k) clearances |
| Nov 20, 2007 | CELLSEARCH CIRCULATING TUMOR CELL KITK071729 · NQI | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
