Research & Development
Caliber Imaging & Diagnostics wins US FDA's 510(k) clearance for its VIVASCOPE System
16 May 2018 -

Caliber Imaging & Diagnostics Inc reported on Tuesday the receipt of the Food and Drug Administration's (FDA) 510(k) clearance for modifications to its non-destructive in-vivo imaging modality, the VIVASCOPE System.

The company said the VIVASCOPE System is an industry-leading reflectance confocal microscopy (RCM) device that allows dermatologists to non-invasively visualize cellular structures within the skin. The recent modifications to the system include refined ergonomics and improved imaging capabilities.

In conjunction, the company's VIVASCOPE System product portfolio has been featured by more than 800 publications. A non-destructive in-vivo imaging modality, the system painlessly provides high-resolution RCM images of the epidermis down to the supporting stroma in thin, optical slices.

Headquartered in Andover, Massachusetts, Caliber Imaging & Diagnostics Inc is a global leader in the design and manufacture of in-vivo and ex-vivo confocal microscopy equipment for the medical device, clinical research and life science industries.

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