Data / Medical devices / System, Microarray-Based, Genome-Wide, Postnatal Chromosomal Abnormality Detection
System, Microarray-Based, Genome-Wide, Postnatal Chromosomal Abnormality Detection (PFX): 6 FDA-registered makers in 3 countries
6 establishments in 3 countries are registered with the FDA to make System, Microarray-Based, Genome-Wide, Postnatal Chromosomal Abnormality Detection (product code PFX, Class 2, 21 CFR 866.5920). 3 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on August 11, 2017, and lists 2 recall events (0 Class I). FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Product code
- PFX
- Device class
- 2
- Regulation
- 866.5920
- Medical specialty
- Immunology
Makers by country
| Country | Makers |
|---|---|
| United States | 4 |
| Singapore | 1 |
| Lithuania | 1 |
Makers of System, Microarray-Based, Genome-Wide, Postnatal Chromosomal Abnormality Detection
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Affymetrix, Inc. | Pleasanton, CA, United States | Manufacturer, Specification developer | 1 | January 17, 2014 | 0 | 0 | 0 | api.fda.gov |
| Agilent Technologies Inc. | Cedar Creek, TX, United States | Complaint file establishment, Manufacturer, Repackager or relabeler | 1 | August 11, 2017 | 0 | 0 | 0 | api.fda.gov |
| Agilent Technologies, Inc | Santa Clara, CA, United States | Manufacturer, Specification developer | 1 | August 11, 2017 | 0 | 1 | 0 | api.fda.gov |
| Life Technologies Holdings Pte Ltd | Jurong West North West, Singapore | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Roche Molecular Systems, Inc. | Branchburg, NJ, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Thermo Fisher Scientific Baltics UAB | Vilnius Vilniaus Miestas, Lithuania | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated August 11, 2017. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.