Data / Medical devices / High Throughput Dna Sequence Analyzer / United States
FDA-registered makers of High Throughput Dna Sequence Analyzer in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make High Throughput Dna Sequence Analyzer (product code PFF). 2 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- High Throughput Dna Sequence Analyzer
- Product code
- PFF
- Country
- United States
Makers of High Throughput Dna Sequence Analyzer in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Illumina, Inc. | San Diego, CA, United States | Complaint file establishment, Manufacturer, Specification developer | 1 | November 19, 2013 | 0 | 6 | 0 | api.fda.gov |
| Illumina, Inc. Hayward | Hayward, CA, United States | Manufacturer | 1 | November 19, 2013 | 0 | 0 | 0 | api.fda.gov |
| Life Technologies Corporation | Austin, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Life Technologies Corporation | S San Fran, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Life Technologies Corporation | Carlsbad, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Life Technologies Corporation | Guilford, CT, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Life Technologies Corporation | Frederick, MD, United States | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| STS Corporation | Duluth, GA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | 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.