Xdx: FDA filings under this applicant name
FDA lists 0 510(k) clearances under the applicant name “Xdx”, plus 1 De Novo decision, across 1 product code in 1 review panel. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| OJQ | Cardiac Allograft Gene Expression Profiling Test System | 1 | 0 |
Review panels
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| DEN080007 | De Novo | Cardiac Allograft Gene Expression Profiling Test System | 2008-08-26 |
Recalls
openFDA lists no recalls under a recalling firm named Xdx.
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Device clinical trials
An industry sponsor named Xdx is the lead sponsor of 1 device studies on ClinicalTrials.gov (0 active or recruiting). Most recent:
- NCT00351559: IMAGE: A Comparison of AlloMap Molecular Testing and Traditional Biopsy-based Surveillance for Heart Transplant Rejection (Completed, started 2005-01)
Frequently asked questions
How many FDA 510(k) clearances are listed under Xdx?
FDA lists 0 510(k) clearances under the applicant name “Xdx”, plus 1 De Novo decision, across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
Which FDA product codes appear under Xdx?
The most frequent FDA product codes under this applicant name are OJQ (Cardiac Allograft Gene Expression Profiling Test System, 1).
Next steps
- See all 0 Xdx clearances with predicates and recalls
- Run predicate analysis for product code OJQ, Xdx's most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.