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
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Freeland Systems, LLC | Carmel, IN, United States | Manufacturer | 1 | March 31, 1997 | 0 | 0 | 0 | api.fda.gov |
| Aspyra, LLC. | Jacksonville, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Apryse Software Corp. | Charlotte, NC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Avnet, Inc. (Avnet Logistics) | Chandler, AZ, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Brit Systems | Wallingford, CT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Codonics, Inc. | Middleburg Heights, OH, United States | Complaint file establishment, Manufacturer, Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Computer MD | Fort Lauderdale, FL, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Conmed Corporation | Utica, NY, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Caliber Imaging & Diagnostics, Inc. | Rochester, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Core Sound Imaging | Raleigh, NC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gyrus Acmi, Inc. | Westborough, MA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Health Care Tech Solutions, LLC | Victoria, MN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| HP Inc | Fort Collins, CO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| IMRIS Imaging, Inc. | Chaska, MN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Digital Developers LLC | New Rochelle, NY, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medicatech Usa | Anaheim, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mim Software Inc. | Cleveland, OH, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| NDS Surgical Imaging, LLC. | Sarasota, FL, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Paxerahealth Corp | Newton, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PENTAX of America, Inc. | Montvale, NJ, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Smith & Nephew Inc. | Oklahoma City, OK, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Smith & Nephew Inc. | Andover, MA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Standard Imaging, Inc. | Middleton, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Endoscopy | San Jose, CA, United States | Manufacturer | 0 | 0 | 2 | 0 | api.fda.gov | |
| Thinking Systems Corp. | Saint Petersburg, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Trillium Technology, Inc | Grass Lake, MI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Trice Imaging, Inc. | Miami, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| VA OI&T/EPMO/TRS/HPS Organization | Washington, DC, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| iCRco Inc. | Goleta, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.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.