Data / Medical devices / Test-Pattern, Radiographic
Test-Pattern, Radiographic (IXF): 12 FDA-registered makers in 5 countries
12 establishments in 5 countries are registered with the FDA to make Test-Pattern, Radiographic (product code IXF, Class 1, 21 CFR 892.1940). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 5 510(k) clearances under this code, the latest on January 12, 1987, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- IXF
- Device class
- 1
- Regulation
- 892.1940
- Medical specialty
- Radiology
Makers by country
| Country | Makers |
|---|---|
| United States | 8 |
| United Kingdom | 1 |
| Poland | 1 |
| France | 1 |
| Mexico | 1 |
Makers of Test-Pattern, Radiographic
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 |
|---|---|---|---|---|---|---|---|---|
| Cortechs Labs, Inc. | Cov, KY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GE Healthcare Coils | Aurora, OH, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ge Medical Systems, LLC | Waukesha, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Leeds Test Objects Ltd | BOROUGHBRIDGE, YORK North Yorkshire, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Phantom Laboratory | Greenwich, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pro-Project | Okszow Lubuskie, Poland | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Qualiformed SAS | La Roche Sur Yon Pays de la Loire, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Radiation Products Design, Inc. | Albertville, MN, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Resoundant, Inc. | Rochester, MN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sun Nuclear Corporation | Norfolk, VA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Welch Allyn De Mexico, S. De R.L. De C.V. | TIJUANA Baja California, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Welch Allyn, Inc. | Skaneateles Falls, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated January 12, 1987. 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.