Devices
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Most establishments that are required to register with the FDA are also required to list the devices that are made there and the activities that are performed on those devices. If ...
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This dataset contains Medical Device Establishment Registration listing including Registration ID and Registration Key. Registration and listing provides FDA with the location of m...
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The Medical Device Reporting dataset contains information from CDRH's device experience reports on devices which may have malfunctioned or caused a death or serious injury. The d...
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This data package contains all (510(k)) submissions for medical devices reviewed by FDA’s Center for Devices and Radiological Health (CDRH), reporting status of post-approval s...
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The Medical Devices Classification dataset contains device names and their associated product codes. The name and product code identify the generic category of a device for FDA. Th...
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The FDA posts consumer information about the most serious medical device recalls. These products are on the list because there is a reasonable chance that they could cause serious ...
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The Medical Product Safety Network dataset involves the reporting of problems with medical products from a network of approximately 300 hospitals, nursing homes and home health fac...
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This dataset is one of the surveys carried out by Dartmouth Atlas under the umbrella "Effective Care". Effective care refers to services that are of proven value and have no signif...
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Radiation-emitting products run the gamut from diagnosing serious medical conditions through such things as X-rays and mammograms to helping ensure the safety of airports and offic...
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The Radiation-Emitting Electronic Products Corrective Actions and Recalls includes electronic products for which manufacturers are required to perform corrective actions when a rad...