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# Body Vision’s LungVision 2.0 System Cleared
- URL: https://www.fdaweb.com/body-visions-lungvision-2-0-system-cleared/
- Published: 2019-05-21T12:00:00.000Z
- Updated: 2026-09-15T01:27:59.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5144157

FDA has cleared a Body Vision Medical 510(k) for the LungVision 2.0 System. The new device features “real-time tool-in-lesion confirmation combined with seamless integration of LungVision Tool, a disposable lung navigation catheter,” according to the company. The LungVision Tool, which is guided by the LungVision 2.0 System, is used through standard bronchoscopes to allow access of any endotherapy accessories to small pulmonary nodules, it says.

The device uses machine learning and for accurate real-time navigation, and it allows physicians to plan, visualize, and track endobronchial tools inside radiolucent lesions in real time, Body Vision says. It also reveals fluoroscopically “blind” lesions during biopsy sampling through any conventional C-Arm, which is widely available in a standard bronchoscopy suite, it says.