
Intalight's DREAM OCT platform receives CE Mark
DREAM is an acronym for deep imaging depth, rapid sweeping speed, extensive scan range, accurate results, and multimodal imaging capabilities.
Ophthalmic technologies company Intalight has announced that its DREAM OCT platform received a CE Mark through the European Union.1 The new version of optical coherence tomography (OCT) “provides the highest quality OCT images currently on the market,” according to a news release.
"Intalight is incredibly proud to receive CE mark approval in Europe for our DREAM OCT," said Intalight Chairman and Founder Shawn Peng in the release. "This achievement allows us to provide ophthalmologists in Europe with state-of-the-art technology that delivers improved results for their patients."
DREAM is an acronym for deep imaging depth, rapid sweeping speed, extensive scan range, accurate results, and multimodal imaging capabilities. The device has the capability of covering an ultrawide single scan, delivering a 130-degree optical coherence tomography angiography (OCTA) image. With swept-source 12 mm super-depth scanning, the DREAM OCT is able to image a large portion of the vitreous space, in addition to providing quality imaging of the choroid and retina. The super-depth anterior scanning achieves 16.2 mm (in air), which allows for the complete anterior segment, from the cornea to the anterior part of the vitreous, to be scanned in a single scan.1 The device’s capabilities for longer wavelength allows for the penetration through opacities in either the lens or vitreous, the release stated.
"Over the past few years, we've heard from eye care professionals that they need a solution that gets them over the imaging finish line with speed, accuracy and depth," said Intalight CEO and Cofounder Bing Li in the release. "DREAM OCT delivers a full set of imaging modalities for the most challenging clinical and research applications for the retina and outperforms everything else health care providers know."
Intalight also noted that more than 160 peer-reviewed papers have utilized findings from DREAM OCT devices thus far.1 One of the most recent studies, published in Retina, examined the macular sensitivity using microperimetry in patients with proliferate
“Postoperative mean macular sensitivity was significantly correlated with outer retinal thickness and deep capillary plexus perfusion for patients with proliferative diabetic retinopathy,” the study authors stated. The authors were led by first author Manqiao Wang, MD, PhD, of Tiangin Key Laboratory of Retinal Function and Diseases, the Tiangin Branch of National Clinical Research Center for Ocular Disease, the Eye Institute and School of Optometry, and the Tianjin Medical University Eye Hospital, all in Tianjin, Chian.2
DREAM OCT devices are currently being utilized in retina academic institutions and retina private practices in the US, Europe, and Asia, according to Intalight.1
"This is such exciting news for Intalight that there's no more waiting in Europe, and we look forward to being able to provide this innovative solution in the US," said Intalight Chief Commercial Officer Joe Garibaldi in the release. "We look forward to continuing to grow our prestigious network of global institutions and ophthalmologists with our recent CE approval and eventually our FDA approval."
References:
Intalight receives CE Mark for its progressive DREAM OCT swept source imaging. News release. PR Newswire. May 15, 2025. Accessed May 19, 2025.
https://www.prnewswire.com/news-releases/intalight-receives-ce-mark-for-its-progressive-dream-oct-swept-source-imaging-302454390.html Wang M, Shao Y, Gong Y, et al. Association of macular structure with microperimetry sensitivity following vitrectomy for proliferate diabetic retinopathy. Retina. 2024;44(6):982-990. doi:10.1097/IAE.0000000000004063
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