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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

CountryMakers
United States8
China4
Germany3
Italy2
Mexico2
Netherlands2
South Korea1
Estonia1
Belgium1
Spain1

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.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Villa Sistemi Medicali S.P.A.BUCCINASCO Milano, ItalyManufacturer1March 25, 2005020api.fda.gov
Anholt Technologies Inc.Avondale, PA, United StatesManufacturer0000api.fda.gov
Baxter Medical Systems (Suzhou) Co. LtdTaicang City Jiangsu, ChinaManufacturer, Specification developer0000api.fda.gov
Baxter Medical Systems GmbH + Co. KGSAALFELD Thuringia, GermanyComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Carestream Health, Inc., Global R&D CenterShanghai, ChinaSpecification developer0000api.fda.gov
Compania Mexicana De Radiologia CGR, S.A. De C.V.Queretaro, MexicoManufacturer0000api.fda.gov
Del Medical, Inc.Bloomingdale, IL, United StatesManufacturer0000api.fda.gov
Domico Med-Device, LLCFenton, MI, United StatesContract manufacturer, Manufacturer0000api.fda.gov
ECOTRON Co., Ltd.Seoul, South KoreaManufacturer0000api.fda.gov
Ge Healthcare (tianjin) Company LimitedTianjin, ChinaSpecification developer0000api.fda.gov
GE Healthcare (China) Co., Ltd.Beijing, ChinaSpecification developer0000api.fda.gov
Ge Medical Systems Monterrey Mexico, S.A. De C.V.APODACA Nuevo Leon, MexicoManufacturer0000api.fda.gov
Ge Medical Systems, LLCWaukesha, WI, United StatesSpecification developer0000api.fda.gov
General Medical Merate S.P.A.Seriate, Bergamo, ItalyManufacturer0000api.fda.gov
Gabriel Scientific OUParnu linn Parnumaa, EstoniaContract manufacturer0000api.fda.gov
IMRIS Imaging, Inc.Chaska, MN, United StatesManufacturer0030api.fda.gov
Livermoretech,incPlano, TX, United StatesManufacturer, Remanufacturer, Repackager or relabeler0000api.fda.gov
Maquet GMBHRASTATT Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov
Mizuho Orthopedic Systems, Inc.Union City, CA, United StatesManufacturer0000api.fda.gov
Orfit Industries NVWIJNEGEM Antwerpen, BelgiumManufacturer0000api.fda.gov
Philips Medical Systems Nederland B.V.BEST Noord-Brabant, NetherlandsComplaint file establishment, Specification developer0000api.fda.gov
Philips Medical Systems Nederland B.V.BEST Noord-Brabant, NetherlandsContract manufacturer0000api.fda.gov
Sedecal S.A.ALGETE Madrid(Province), SpainManufacturer0000api.fda.gov
Surgical Tables IncorporatedMiddleton, MA, United StatesManufacturer0000api.fda.gov
Siemens Healthineers AGKEMNATH Bavaria, GermanyManufacturer0000api.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.