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Data / Medical devices / Device, Digital Image Storage, Radiological / United States

FDA-registered makers of Device, Digital Image Storage, Radiological in the United States: 29 establishments

29 establishments in the United States are registered with the FDA to make Device, Digital Image Storage, Radiological (product code LMB). 1 has a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Device, Digital Image Storage, Radiological
Product code
LMB
Country
United States

Makers of Device, Digital Image Storage, Radiological in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Freeland Systems, LLCCarmel, IN, United StatesManufacturer1March 31, 1997000api.fda.gov
Aspyra, LLC.Jacksonville, FL, United StatesManufacturer0000api.fda.gov
Apryse Software Corp.Charlotte, NC, United StatesManufacturer0000api.fda.gov
Avnet, Inc. (Avnet Logistics)Chandler, AZ, United StatesContract manufacturer0000api.fda.gov
Brit SystemsWallingford, CT, United StatesManufacturer0000api.fda.gov
Codonics, Inc.Middleburg Heights, OH, United StatesComplaint file establishment, Manufacturer, Remanufacturer0000api.fda.gov
Computer MDFort Lauderdale, FL, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Conmed CorporationUtica, NY, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Caliber Imaging & Diagnostics, Inc.Rochester, NY, United StatesManufacturer0000api.fda.gov
Core Sound ImagingRaleigh, NC, United StatesManufacturer0000api.fda.gov
Gyrus Acmi, Inc.Westborough, MA, United StatesSpecification developer0000api.fda.gov
Health Care Tech Solutions, LLCVictoria, MN, United StatesManufacturer0000api.fda.gov
HP IncFort Collins, CO, United StatesSpecification developer0000api.fda.gov
IMRIS Imaging, Inc.Chaska, MN, United StatesManufacturer0000api.fda.gov
Medical Digital Developers LLCNew Rochelle, NY, United StatesSpecification developer0000api.fda.gov
Medicatech UsaAnaheim, CA, United StatesManufacturer0000api.fda.gov
Mim Software Inc.Cleveland, OH, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
NDS Surgical Imaging, LLC.Sarasota, FL, United StatesManufacturer, Specification developer0000api.fda.gov
Paxerahealth CorpNewton, MA, United StatesManufacturer0000api.fda.gov
PENTAX of America, Inc.Montvale, NJ, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Smith & Nephew Inc.Oklahoma City, OK, United StatesManufacturer0000api.fda.gov
Smith & Nephew Inc.Andover, MA, United StatesSpecification developer0000api.fda.gov
Standard Imaging, Inc.Middleton, WI, United StatesManufacturer0000api.fda.gov
Stryker EndoscopySan Jose, CA, United StatesManufacturer0020api.fda.gov
Thinking Systems Corp.Saint Petersburg, FL, United StatesManufacturer0000api.fda.gov
Trillium Technology, IncGrass Lake, MI, United StatesManufacturer0000api.fda.gov
Trice Imaging, Inc.Miami, FL, United StatesManufacturer0000api.fda.gov
VA OI&T/EPMO/TRS/HPS OrganizationWashington, DC, United StatesSpecification developer0000api.fda.gov
iCRco Inc.Goleta, CA, United StatesManufacturer0000api.fda.gov

Updated November 2, 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.