Data / Medical devices / Display, Cathode-Ray Tube, Medical / United States
FDA-registered makers of Display, Cathode-Ray Tube, Medical in the United States: 12 establishments
12 establishments in the United States are registered with the FDA to make Display, Cathode-Ray Tube, Medical (product code DXJ). 9 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Display, Cathode-Ray Tube, Medical
- Product code
- DXJ
- Country
- United States
Makers of Display, Cathode-Ray Tube, Medical in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Arthrex, Inc. | Naples, FL, United States | Specification developer | 2 | February 22, 2018 | 0 | 0 | 0 | api.fda.gov |
| Zoll Medical Corporation | Chelmsford, MA, United States | Complaint file establishment, Manufacturer | 2 | April 3, 2014 | 0 | 0 | 0 | api.fda.gov |
| Carrot Medical, LLC | Bothell, WA, United States | Manufacturer, Specification developer | 1 | November 26, 2008 | 0 | 0 | 0 | api.fda.gov |
| GE Medical Systems Information Technologies, Inc. | Waukesha, WI, United States | Specification developer | 1 | September 15, 2016 | 0 | 0 | 0 | api.fda.gov |
| GE Medical Systems Information Technologies, Inc. | Wauwatosa, WI, United States | Specification developer | 1 | September 15, 2016 | 0 | 0 | 0 | api.fda.gov |
| Murata Vios, Inc. | Woodbury, MN, United States | Complaint file establishment, Manufacturer, Remanufacturer, Repackager or relabeler | 1 | July 26, 2018 | 0 | 0 | 0 | api.fda.gov |
| Philips North America LLC | Cambridge, MA, United States | Complaint file establishment, Specification developer | 1 | October 30, 2015 | 0 | 0 | 0 | api.fda.gov |
| Philips North America LLC | Andover, MA, United States | Specification developer | 1 | October 30, 2015 | 0 | 6 | 0 | api.fda.gov |
| St. Jude Medical, Atrial Fibrillation Division, Inc. | Saint Paul, MN, United States | Specification developer | 1 | January 26, 2011 | 0 | 0 | 0 | api.fda.gov |
| Arthrex, Inc. | Ave Maria, FL, United States | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Covidien | Lafayette, CO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips North America LLC | Export, PA, United States | Contract manufacturer | 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.