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https://orthospinenews.com/2026/03/31/restore-robotics-receives-fda-510k-clearance-for-two-additional-da-vinci-xi-robotic-instruments/ Restore Robotics Receives FDA 510(k) Clearance for Two Additional da Vinci Xi® Robotic Instruments... receives fda 510 k clearance two additional restore robotics https://diagnostics.roche.com/us/en/news-listing/2026/fda-cobas-c-703-cobas-ise-neo.html Roche receives FDA 510(k) clearance for bcobas/b® c 703 and bcobas/b® ISE neo,... receives fda 510 k clearance roche 703 ise https://atdc.org/us-food-and-drug-administration-gives-huxley-medical-510k-clearance-for-sansa-home-sleep-apnea-test/ Huxley Medical Receives FDA 510(k) | ATDC Member Company Dec 2, 2025 - Huxley Medical earns FDA 510(k) clearance for SANSA, the first chest-worn AI-powered home sleep apnea diagnostic patch improving patient outcomes. receives fda 510 atdc member company huxley medical k https://www.biospace.com/epitel-receives-fda-510-k-clearance-for-two-new-technologies-remi-remote-eeg-monitoring-system-for-ambulatory-use-and-remi-vigilenz-ai-for-event-detection Epitel Receives FDA 510(k) Clearance for Two New Technologies: REMI Remote EEG Monitoring System... Apr 24, 2024 - Epitel, a leader in AI technologies for patient-focused brain health solutions, announced today it received U.S. Food and Drug Administration (FDA) 510(k)... receives fda 510 k clearance two new monitoring system https://www.prweb.com/releases/spinepoint-receives-us-fda-510k-clearance-for-flex-z-cervical-cage-first-product-in-the-ultra-low-stiffness-cushioning-interbody-platform-302725995.html SpinePoint Receives U.S. FDA 510(k) Clearance for Flex-Z™ Cervical Cage/ First Product in the... Mar 27, 2026 - /PRNewswire-PRWeb/ -- SpinePoint LLC, a medical device company developing low stiffness cushioning spinal interbody cages through advanced additive... fda 510 k receives u cage first clearance flex