Home › Device types › LMD
System, Digital Image Communications, Radiological
FDA product code LMD · Class 1 · Radiology
499
Registered devices
168
Adverse events
12
Recalls
142
510(k) clearances
Devices with this code
QG-TV-IP-FM — CARESTREAM HEALTH, INC.Vitrea Advanced Visualization — Canon Medical Informatics, Inc.OmnifyXR — Mediview Xr, Inc.Eureka — Terarecon Inc.PowerLook PRO+ 4GPU Tower Platform, OUS — Icad, Inc.ViewBox Basic — RadiusOptiVu Streamer — INCREMED AGDICOM Proxy — Brainlab SEEBM — EBM TECHNOLOGIES INCORPORATEDVitrea View — Canon Medical Informatics, Inc.ScaleOR — Nds Surgical Imaging LLCVitrea Advanced Visualization — Canon Medical Informatics, Inc.interWORKS — Avreo IncEonis 19” — Barco NVCenova — Hologic, Inc.PowerLook PRO+ Rack-Mount, US — Icad, Inc.MediCap — MEDICAPTURE, INC.MVC — MEDICAPTURE, INC.Lilly Together — ELI LILLY AND COMPANYVitrea Read — Canon Medical Informatics A/SVitrea Advanced Visualization — Canon Medical Informatics, Inc.EasyViz — Canon Medical Informatics A/SAmbra Health Mobile Application — Ambra HealthRadiology Information Systems, Inc. — Radiology Information Systems, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-09-11 | Skytron, Div. The KMW Group, Inc | VGDF (VGA) Faceplate failure results in failure of video signal for SkyVision Linx 300, a secondary display. Video would continue on the primary source device d |
| 2020-03-10 | Skytron, Div. The KMW Group, Inc | Intermittent failure of a signal being sent to a monitor from the touch panel display causing the displaying monitor to go Blank and the touch panel to displa |
| 2015-12-04 | CompView Medical, LLC | The attachment of the NuCART Spring Arm to the NuCART horizontal boom may come apart if the securing ring (snap ring) was not installed correctly causing the sp |
| 2015-05-06 | Siemens Medical Solutions USA, Inc | A potential exists for order transactions from interfaced HIS (Hospital Information System) systems to be lost during a restart of interface processes when usin |
| 2014-06-25 | Karl Storz Endoscopy | KARL STORZ Endoscopy-America is recalling the Essential NEO because the connected power cable could potentially become overheated and result in smoke being gene |
| 2012-04-19 | Ge Healthcare It | GE Healthcare has become aware of an issue associated with rejected images using the WADO protocol within GE Centricity Web that may impact patient safety. The |
| 2009-12-11 | Stryker Endoscopy | Device will not able to assign the correct time/date stamp for saved filed after December 31, 2009. On Jan 1, 2010, the device system date for all SDC Pro 2 un |
| 2008-12-12 | GE Healthcare Integrated IT Solutions | Software error: There are two potential safety situations with Centricity Enterprise Web software - a forced log off may occur while using the Centricity Enterp |
| 2007-12-11 | AGFA Corp. | Failure of Data Transmission: No imaging data could be transmitted by the device, because a key value needed for data transmission was incorrectly entered in t |
| 2007-05-02 | Siemens Medical Solutions USA, Inc | System could crash and result in data loss. |
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