Data / Medical devices / Barrier, Control Panel, X-Ray, Movable

Barrier, Control Panel, X-Ray, Movable (IWX): 18 FDA-registered makers in 8 countries

Name: FDA-registered makers of Barrier, Control Panel, X-Ray, Movable
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

18 establishments in 8 countries are registered with the FDA to make Barrier, Control Panel, X-Ray, Movable (product code IWX, Class 1, 21 CFR 892.6500). 0 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 3 510(k) clearances under this code, the latest on April 27, 1988, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.

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Product code: IWX
Device class: 1
Regulation: 892.6500
Medical specialty: Radiology

Makers by country

Country	Makers
United States	9
China	3
New Zealand	1
France	1
United Kingdom	1
Germany	1
India	1
Sweden	1

Makers of Barrier, Control Panel, X-Ray, Movable

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	Recall events	Source
Aadco Medical, Inc.	Randolph, VT, United States	Manufacturer	1	api.fda.gov
Adept Medical Ltd	Auckland, New Zealand	Manufacturer	0	api.fda.gov
BGSS Company Asia Limited	Zhabei Shanghai, China	Manufacturer	0	api.fda.gov
Cardio Medical Products, Inc.	Rockaway, NJ, United States	Specification developer	0	api.fda.gov
Ge Medical Systems SCS	Buc, France	Specification developer	0	api.fda.gov
Image Diagnostics, Inc.	Fitchburg, MA, United States	Manufacturer	0	api.fda.gov
Intech Partners LLC	Oak Ridge North, TX, United States	Repackager or relabeler, Specification developer	0	api.fda.gov
Kenex (electro-Medical) Ltd.	HARLOW Essex, United Kingdom	Manufacturer	0	api.fda.gov
Mavig GMBH	MUNICH Bavaria, Germany	Manufacturer	0	api.fda.gov
Medipack Medical Packaging MFG. Co.	DONGGUAN CITY Guangdong, China	Manufacturer	0	api.fda.gov
MPS Project	New Delhi, India	Manufacturer	0	api.fda.gov
Phillips Safety Products, Inc.	Middlesex, NJ, United States	Manufacturer	0	api.fda.gov
Protech Leaded Eyewear, Inc.	West Palm Beach, FL, United States	Manufacturer, Specification developer	0	api.fda.gov
Techno-Aide, Inc.	Whites Creek, TN, United States	Manufacturer	0	api.fda.gov
Texray AB	Goteborg Vastra Gotaland, Sweden	Manufacturer	0	api.fda.gov
Tianjin Kanghuajianye Medical Materials Co., Ltd.	Tianjin, China	Contract manufacturer, Manufacturer	0	api.fda.gov
Weslacova	North Wilkesboro, NC, United States	Contract manufacturer	0	api.fda.gov
Wolf X-Ray Corp	Battleboro, NC, United States	Manufacturer, Repackager or relabeler	0	api.fda.gov

Updated April 27, 1988. 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.