Data / Medical devices / Phantom, Anthropomorphic, Radiographic

Phantom, Anthropomorphic, Radiographic (IXG): 20 FDA-registered makers in 6 countries

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

20 establishments in 6 countries are registered with the FDA to make Phantom, Anthropomorphic, Radiographic (product code IXG, Class 1, 21 CFR 892.1950). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 4 510(k) clearances under this code, the latest on September 19, 1991, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code: IXG
Device class: 1
Regulation: 892.1950
Medical specialty: Radiology

Makers by country

Country	Makers
United States	14
Germany	2
China	1
France	1
Australia	1
Switzerland	1

Makers of Phantom, Anthropomorphic, 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	Source
Ashland Specialty Ingredients, G.P.	Bridgewater, NJ, United States	Manufacturer	api.fda.gov
Anholt Technologies Inc.	Avondale, PA, United States	Manufacturer	api.fda.gov
Cortex Manufacturing, LLC	Byhalia, MS, United States	Manufacturer	api.fda.gov
Dentsply LLC	York, PA, United States	Manufacturer	api.fda.gov
Ge Medical Systems, LLC	Waukesha, WI, United States	Specification developer	api.fda.gov
Guangdong Meicen Medical Equipment Co., Ltd.	foshan Guangdong, China	Manufacturer	api.fda.gov
IBA Dosimetry GmbH	SCHWARZENBRUCK Bavaria, Germany	Manufacturer	api.fda.gov
Medtec LLC	Orange City, IA, United States	Manufacturer	api.fda.gov
Phantom Laboratory	Greenwich, NY, United States	Manufacturer	api.fda.gov
Polygel LLC.	Palmer TWP, PA, United States	Specification developer	api.fda.gov
PTW Freiburg	FREIBURG Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Qualiformed SAS	La Roche Sur Yon Pays de la Loire, France	Manufacturer	api.fda.gov
Resonance Health Analysis Services Pty Ltd	Burswood Western Australia, Australia	Manufacturer	api.fda.gov
Smith & Nephew, Inc.	Memphis, TN, United States	Manufacturer	api.fda.gov
Standard Imaging, Inc.	Middleton, WI, United States	Contract manufacturer, Manufacturer	api.fda.gov
Sun Nuclear Corporation	Melbourne, FL, United States	Manufacturer	api.fda.gov
Smith & Nephew, Inc.	Memphis, TN, United States	Manufacturer	api.fda.gov
Sun Nuclear Corporation	Norfolk, VA, United States	Contract manufacturer, Manufacturer, Specification developer	api.fda.gov
Varian Medical Systems Imaging Laboratory GmbH	Daettwil, Argovia Aargau, Switzerland	Complaint file establishment, Specification developer	api.fda.gov
Varian Medical Systems, Inc.	San Jose, CA, United States	Manufacturer	api.fda.gov

Updated September 19, 1991. 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.