Data / Medical devices / Kit, Dna Detection, Human Papillomavirus / United States
FDA-registered makers of Kit, Dna Detection, Human Papillomavirus in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Kit, Dna Detection, Human Papillomavirus (product code MAQ). 6 have a 510(k) clearance or PMA approval on file and 5 have a recall event. FDA data exported November 2, 2026.
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- Device
- Kit, Dna Detection, Human Papillomavirus
- Product code
- MAQ
- Country
- United States
Makers of Kit, Dna Detection, Human Papillomavirus in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Roche Molecular Systems, Inc. | Branchburg, NJ, United States | Manufacturer, Manufacturer for export | 0 | 2 | 2 | 0 | api.fda.gov | |
| Roche Molecular Systems, Inc. | Pleasanton, CA, United States | Specification developer | 0 | 2 | 0 | 0 | api.fda.gov | |
| Abbott Molecular, Inc. | Des Plaines, IL, United States | Manufacturer, Manufacturer for export | 0 | 1 | 1 | 0 | api.fda.gov | |
| Abbott Molecular Distribution Center | Itasca, IL, United States | Manufacturer, Manufacturer for export | 0 | 1 | 0 | 0 | api.fda.gov | |
| Becton, Dickinson & Co. | Sparks, MD, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 1 | 2 | 0 | api.fda.gov | |
| Qiagen | Germantown, MD, United States | Manufacturer, Manufacturer for export, Specification developer | 0 | 1 | 1 | 0 | api.fda.gov | |
| Autogenomics, Incorporated | Carlsbad, CA, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Promega Corporation | Madison, WI, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ventana Medical Systems, Inc. | Tucson, AZ, United States | Manufacturer for export | 0 | 0 | 1 | 1 | api.fda.gov |
Updated November 2, 2026. 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.