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# Noah Medical’s Robotic Bronchoscopy Device Cleared
- URL: https://www.fdaweb.com/noah-medicals-robotic-bronchoscopy-device-cleared/
- Published: 2023-03-02T12:00:00.000Z
- Updated: 2026-09-14T18:17:57.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5153897

FDA has cleared a Noah Medical 510(k) for the Galaxy System, a robotic-navigated bronchoscopy device and accessories that are intended to provide bronchoscopic visualization and access to patient airways for diagnostic and therapeutic procedures. The company says the majority of cancerous lesions are located in the outer third area of the lung, which is more difficult for doctors to reach for biopsy. “The Galaxy System’s advanced imaging technologies provide real-time location updates,” it says, “and are designed to improve tool-in-lesion and diagnostic yield.”

The device features “TiLT Technology” with integrated tomosynthesis and augmented fluoroscopy, Noah says. “With its always-on-camera bronchoscope, direct visualization is enabled for the entire procedure, including at the time of biopsy,” it says, adding that the device’s four-way bronchoscope articulation allows navigation to most peripheral lesions.