Data / Medical devices / Table, Radiographic, Stationary Top

Table, Radiographic, Stationary Top (IXQ): 19 FDA-registered makers in 9 countries

Name: FDA-registered makers of Table, Radiographic, Stationary Top
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

19 establishments in 9 countries are registered with the FDA to make Table, Radiographic, Stationary Top (product code IXQ, Class 2, 21 CFR 892.1980). 2 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 27 510(k) clearances under this code, the latest on December 5, 1997, and lists 3 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code: IXQ
Device class: 2
Regulation: 892.1980
Medical specialty: Radiology

Makers by country

Country	Makers
United States	8
Germany	3
Japan	2
Sweden	1
India	1
Canada	1
Netherlands	1
Spain	1
Serbia	1

Makers of Table, Radiographic, Stationary Top

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	Recall events	Source
Anholt Technologies Inc.	Avondale, PA, United States	Manufacturer	1	December 5, 1997	0	api.fda.gov
Medtec LLC	Orange City, IA, United States	Manufacturer	1	December 5, 1997	2	api.fda.gov
3C-Medical Intelligence GmbH	Landsberg am Lech Bavaria, Germany	Manufacturer	0		0	api.fda.gov
Accogent Pausch	Eatontown, NJ, United States	Manufacturer	0		0	api.fda.gov
Core Labs, LLC.	Englewood, CO, United States	Manufacturer	0		0	api.fda.gov
Diacor, Inc.	Mount Pleasant, UT, United States	Manufacturer	0		0	api.fda.gov
Elekta Solutions AB	Stockholm, Sweden	Manufacturer	0		0	api.fda.gov
Greens Surgicals Private Limited	Vadodara Gujarat, India	Manufacturer	0		0	api.fda.gov
Maquet GMBH	RASTATT Baden-Wurttemberg, Germany	Manufacturer	0		0	api.fda.gov
Oakworks, Inc.	New Freedom, PA, United States	Manufacturer	0		0	api.fda.gov
Octostop, Inc.	LAVAL Quebec, Canada	Manufacturer	0		0	api.fda.gov
Philips Medical Systems Nederland B.V.	BEST Noord-Brabant, Netherlands	Contract manufacturer	0		0	api.fda.gov
Philips Medical Systems DMC GmbH	Hamburg, Germany	Complaint file establishment, Specification developer	0		0	api.fda.gov
Radiation Products Design, Inc.	Albertville, MN, United States	Manufacturer, Repackager or relabeler	0		0	api.fda.gov
Sedecal S.A.	ALGETE Madrid(Province), Spain	Manufacturer	0		0	api.fda.gov
Shimadzu Corporation Medical Systems Division	Kyoto, Japan	Manufacturer	0		0	api.fda.gov
Shimane Shimadzu Corporation	IZUMO Shimane, Japan	Manufacturer	0		0	api.fda.gov
Summit Industries, LLC	Niles, IL, United States	Complaint file establishment, Manufacturer	0		0	api.fda.gov
Visaris D.O.O.	Zemun Beograd, Serbia	Manufacturer	0		0	api.fda.gov

Updated December 5, 1997. 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.