Data / Medical devices / Instrument, Quality-Assurance, Radiologic / United States

FDA-registered makers of Instrument, Quality-Assurance, Radiologic in the United States: 22 establishments

Name: FDA-registered makers of Instrument, Quality-Assurance, Radiologic in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

22 establishments in the United States are registered with the FDA to make Instrument, Quality-Assurance, Radiologic (product code LHO). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device: Instrument, Quality-Assurance, Radiologic
Product code: LHO
Country: United States

Makers of Instrument, Quality-Assurance, Radiologic in the United States

Maker	Location	Role	510(k) clearances	Latest clearance	Source
Standard Imaging, Inc.	Middleton, WI, United States	Manufacturer	1	November 15, 2004	api.fda.gov
Accumetra	Clifton Park, NY, United States	Complaint file establishment, Manufacturer	0		api.fda.gov
Aktina Medical Corp.	Congers, NY, United States	Manufacturer	0		api.fda.gov
Ashland	Columbus, OH, United States	Manufacturer	0		api.fda.gov
Ashland Specialty Ingredients, G.P.	Bridgewater, NJ, United States	Specification developer	0		api.fda.gov
Accuray Incorporated	Madison, WI, United States	Manufacturer	0		api.fda.gov
Anholt Technologies Inc.	Avondale, PA, United States	Manufacturer	0		api.fda.gov
Ashland Specialty Ingredients, G.P.	Fiskeville, RI, United States	Manufacturer	0		api.fda.gov
Blue Physics	Lutz, FL, United States	Manufacturer	0		api.fda.gov
Ge Medical Systems, LLC	Waukesha, WI, United States	Manufacturer	0		api.fda.gov
Instrumental Machine & Development, Inc.	Warsaw, IN, United States	Contract manufacturer	0		api.fda.gov
Leo Cancer Care Incorporated	Middleton, WI, United States	Complaint file establishment, Manufacturer	0		api.fda.gov
Medtec LLC	Orange City, IA, United States	Manufacturer	0		api.fda.gov
Orthogrid Systems, Inc	Midvale, UT, United States	Complaint file establishment, Manufacturer	0		api.fda.gov
Quality Electrodynamics	Mayfield Village, OH, United States	Complaint file establishment, Manufacturer, Specification developer	0		api.fda.gov
Radcal	Monrovia, CA, United States	Manufacturer	0		api.fda.gov
Radiation Products Design, Inc.	Albertville, MN, United States	Manufacturer, Repackager or relabeler	0		api.fda.gov
Sun Nuclear Corporation	Melbourne, FL, United States	Manufacturer	0		api.fda.gov
SolVIS INC.	Louisville, TN, United States	Manufacturer	0		api.fda.gov
Sun Nuclear Corporation	Norfolk, VA, United States	Contract manufacturer, Manufacturer, Specification developer	0		api.fda.gov
Velmeni	Sunnyvale, CA, United States	Manufacturer	0		api.fda.gov
Varian Medical Systems, Inc	Palo Alto, CA, United States	Manufacturer	0		api.fda.gov

Updated November 3, 2026. 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.