Data / Medical devices / Radioimmunoassay, Free Thyroxine
Radioimmunoassay, Free Thyroxine (CEC): 24 FDA-registered makers in 7 countries
24 establishments in 7 countries are registered with the FDA to make Radioimmunoassay, Free Thyroxine (product code CEC, Class 2, 21 CFR 862.1695). 18 of them have a 510(k) clearance or PMA approval on file and 4 have a recall event. The FDA has issued 92 510(k) clearances under this code, the latest on March 6, 2024, and lists 10 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
- CEC
- Device class
- 2
- Regulation
- 862.1695
- Medical specialty
- Clinical Chemistry
Makers by country
| Country | Makers |
|---|---|
| United States | 12 |
| Ireland | 3 |
| Germany | 3 |
| South Korea | 2 |
| United Kingdom | 2 |
| Italy | 1 |
| Japan | 1 |
Makers of Radioimmunoassay, Free Thyroxine
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 |
|---|---|---|---|---|---|---|---|---|
| Siemens Healthcare Diagnostics Inc. | Newark, DE, United States | Complaint file establishment, Manufacturer, Specification developer | 3 | November 26, 2014 | 0 | 1 | 0 | api.fda.gov |
| Abbott Ireland Diagnostics Division | Longford, Ireland | Manufacturer | 2 | October 27, 2017 | 0 | 1 | 0 | api.fda.gov |
| Beckman Coulter, Inc. | Chaska, MN, United States | Manufacturer | 2 | March 6, 2024 | 0 | 0 | 0 | api.fda.gov |
| Roche Diagnostics GMBH | MANNHEIM Baden-Wurttemberg, Germany | Manufacturer, Repackager or relabeler | 2 | April 7, 2023 | 0 | 0 | 0 | api.fda.gov |
| Siemens Healthcare Diagnostics Inc. | Tarrytown, NY, United States | Complaint file establishment, Specification developer | 2 | September 13, 2013 | 0 | 1 | 0 | api.fda.gov |
| DRG Instruments GMBH | MARBURG Hesse, Germany | Complaint file establishment, Manufacturer | 1 | April 5, 2002 | 0 | 0 | 0 | api.fda.gov |
| DiaSorin Italia S.p.A. | SALUGGIA Vercelli, Italy | Manufacturer | 1 | April 4, 2013 | 0 | 0 | 0 | api.fda.gov |
| Diagnostic Automation/ Cortez Diagnostics Inc,. | Woodland Hills, CA, United States | Manufacturer | 1 | April 5, 2002 | 0 | 0 | 0 | api.fda.gov |
| Monobind, Inc. | Lake Forest, CA, United States | Manufacturer, Manufacturer for export | 1 | April 5, 2002 | 0 | 0 | 0 | api.fda.gov |
| MP Biomedicals Diagnostics Division | Solon, OH, United States | Manufacturer | 1 | January 12, 1983 | 0 | 0 | 0 | api.fda.gov |
| Nanoentek Inc | Hwaseong Gyeonggi, South Korea | Manufacturer | 1 | February 17, 2016 | 0 | 0 | 0 | api.fda.gov |
| Nanoentek Inc | Seoul, South Korea | Specification developer | 1 | February 17, 2016 | 0 | 0 | 0 | api.fda.gov |
| Ortho-Clinical Diagnostics, Inc. | Rochester, NY, United States | Complaint file establishment, Specification developer | 1 | March 18, 1997 | 0 | 0 | 0 | api.fda.gov |
| Ortho-Clinical Diagnostics | Pencoed Bridgend, United Kingdom | Manufacturer | 1 | March 18, 1997 | 0 | 0 | 0 | api.fda.gov |
| Qualigen, Inc. | Carlsbad, CA, United States | Manufacturer | 1 | July 3, 2003 | 0 | 1 | 0 | api.fda.gov |
| Siemens Healthcare Diagnostics Products Limited | LLANBERIS Wales, United Kingdom | Manufacturer | 1 | August 16, 1993 | 0 | 0 | 0 | api.fda.gov |
| Siemens Healthcare Diagnostics Inc. | E Walpole, MA, United States | Manufacturer | 1 | September 13, 2013 | 0 | 0 | 0 | api.fda.gov |
| Tosoh Aia, Inc. | Toyama, Japan | Manufacturer | 1 | September 10, 1991 | 0 | 0 | 0 | api.fda.gov |
| Beckman Coulter Ireland Inc | O CALLAGHANS MILLS Clare, Ireland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| DiaSorin Deutschland GmbH | Dietzenbach Hesse, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Epitope Diagnostics, Inc. | San Diego, CA, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Immunocentrix Corporation | Canoga Park, CA, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Scientific Supplies & Technology, Inc. | Doral, FL, United States | Remanufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Healthcare Diagnostics Manufacturing Ltd. | SWORDS Dublin(County), Ireland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated March 6, 2024. 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.