Data / Medical devices / Table, Radiologic
Table, Radiologic (KXJ): 25 FDA-registered makers in 10 countries
25 establishments in 10 countries are registered with the FDA to make Table, Radiologic (product code KXJ, Class 2, 21 CFR 892.1980). 1 of them has a 510(k) clearance or PMA approval on file and 2 have a recall event. The FDA has issued 31 510(k) clearances under this code, the latest on March 25, 2005, and lists 12 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- KXJ
- Device class
- 2
- Regulation
- 892.1980
- Medical specialty
- Radiology
Makers by country
| Country | Makers |
|---|---|
| United States | 8 |
| China | 4 |
| Germany | 3 |
| Italy | 2 |
| Mexico | 2 |
| Netherlands | 2 |
| South Korea | 1 |
| Estonia | 1 |
| Belgium | 1 |
| Spain | 1 |
Makers of Table, Radiologic
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 |
|---|---|---|---|---|---|---|---|---|
| Villa Sistemi Medicali S.P.A. | BUCCINASCO Milano, Italy | Manufacturer | 1 | March 25, 2005 | 0 | 2 | 0 | api.fda.gov |
| Anholt Technologies Inc. | Avondale, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Baxter Medical Systems (Suzhou) Co. Ltd | Taicang City Jiangsu, China | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Baxter Medical Systems GmbH + Co. KG | SAALFELD Thuringia, Germany | Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Carestream Health, Inc., Global R&D Center | Shanghai, China | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Compania Mexicana De Radiologia CGR, S.A. De C.V. | Queretaro, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Del Medical, Inc. | Bloomingdale, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Domico Med-Device, LLC | Fenton, MI, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ECOTRON Co., Ltd. | Seoul, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ge Healthcare (tianjin) Company Limited | Tianjin, China | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GE Healthcare (China) Co., Ltd. | Beijing, China | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ge Medical Systems Monterrey Mexico, S.A. De C.V. | APODACA Nuevo Leon, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ge Medical Systems, LLC | Waukesha, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| General Medical Merate S.P.A. | Seriate, Bergamo, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gabriel Scientific OU | Parnu linn Parnumaa, Estonia | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| IMRIS Imaging, Inc. | Chaska, MN, United States | Manufacturer | 0 | 0 | 3 | 0 | api.fda.gov | |
| Livermoretech,inc | Plano, TX, United States | Manufacturer, Remanufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Maquet GMBH | RASTATT Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mizuho Orthopedic Systems, Inc. | Union City, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Orfit Industries NV | WIJNEGEM Antwerpen, Belgium | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips Medical Systems Nederland B.V. | BEST Noord-Brabant, Netherlands | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips Medical Systems Nederland B.V. | BEST Noord-Brabant, Netherlands | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sedecal S.A. | ALGETE Madrid(Province), Spain | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Surgical Tables Incorporated | Middleton, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Healthineers AG | KEMNATH Bavaria, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated March 25, 2005. 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.