510 k clearance - Robuta Search

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://www.medtechdive.com/news/mayo-clinic-spinout-510k-heart-failure-screening-a/695281/ Mayo Clinic partner earns 510(k) clearance for heart failure screening algorithm | MedTech Dive The algorithm analyzes 12-lead ECGs to show if a patient may be developing heart failure. 510 k clearance mayo clinic heart failure medtech dive partner https://us.cmrsurgical.com/news/cmr-surgical-secures-510k-clearance-of-its-versius-plus-robotic-surgical-system CMR Surgical secures 510(k) clearance of its Versius Plus robotic surgical system - CMR Surgical Dec 17, 2025 - Regulatory clearance of CMR’s most advanced system paves the way for upcoming US commercial launch. 510 k clearance cmr surgical robotic system secures plus https://www.prweb.com/releases/theodent-secures-fda-510k-clearance-for-rennou-varnish-the-first-professional-fluoride-free-cavity-varnish-authorized-in-the-us-302480847.html Theodent secures FDA 510(k) clearance for Rennou® Varnish, the first professional fluoride-free... fda 510 k first professional fluoride free secures clearance https://www.hairfacts.com/tips/govregs/fda-510k-clearance-tweezer-type-epilators/ FDA 510(k) clearance: Tweezer-type epilators – HairFacts | Hair Removal Information FDA 510(k) clearances: Electric tweezers Beginning on 28 May 1976, the US Food and Drug Administration (FDA) began requiring new medical devices to demonstrate... fda 510 k hairfacts hair removal clearance tweezer type 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