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# Carestream Dual-Energy Imaging Cleared
- URL: https://www.fdaweb.com/carestream-dual-energy-imaging-cleared/
- Published: 2019-11-20T12:00:00.000Z
- Updated: 2026-09-14T15:53:45.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5145555

FDA has cleared a Carestream 510(k) for its Dual-Energy imaging technology and its Focus 35C Detector with [Image Suite Software](https://cts.businesswire.com/ct/CT?id=smartlink&url=https%3A%2F%2Fwww.carestream.com%2Fen%2Fus%2Fmedical%2Fproducts%2Fradiography%2Fcarestream-radiography-software%2Fcarestream-image-suite-v4&esheet=52132473&newsitemid=20191120005236&lan=en-US&anchor=Image+Suite+Software&index=1&md5=06475f5f5c278d3514ce4089ac78dd9c&ref=fdaweb.com) for medical imaging. The company says the device uses two filter materials that are automatically switched between the high- and low-energy exposures to produce a soft-tissue-only image with bone structures removed, as well as a corresponding bone-only image. “This differential filter approach optimizes both X-ray spectrums, achieving optimal dose efficiency,” it says. Carestream’s Dual-Energy technology has also been cleared for chest X-rays on its [DRX-Evolution Plus System](https://cts.businesswire.com/ct/CT?id=smartlink&url=https%3A%2F%2Fwww.carestream.com%2Fen%2Fus%2Fmedical%2Fproducts%2Fradiography%2Fdr-systems%2Fcarestream-drx-evolution-plus&esheet=52132473&newsitemid=20191120005236&lan=en-US&anchor=DRX-Evolution+Plus+System&index=3&md5=4e9b1a36e3da597802484068212bb08f&ref=fdaweb.com).