fda 510 k - 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.hairfacts.com/tips/govregs/fda-510k-intended-use-statements-ndyag-lasers/ FDA 510(k) Intended use statements: Nd:YAG lasers – HairFacts | Hair Removal Information 510(k) intended use statements: Nd:YAG lasers Below is a list of Nd:YAG lasers cleared by FDA. The intended use of each is quoted verbatim from FDA clearances,... fda 510 k hairfacts hair removal intended use statements yag https://airsmed.com/en/swiftmr-oemdl/ SwiftMR® with OEM DL solutions: Now FDA 510(k)-Cleared - AIRS Medical Inc. Apr 28, 2026 - SwiftMR is now FDA-cleared to work alongside OEM deep learning solutions. Reduce MRI scan times further, expand coverage to all sequences and body parts. fda 510 k airs medical oem dl solutions 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.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 https://www.medtechdive.com/news/pulse-seeks-fda-approval-pfa-clamp/720806/ Pulse drops 510(k) plan for PFA device after FDA requests clinical data | MedTech Dive Analysts said the AFib device is now unlikely to come to market before late 2026. 510 k clinical data medtech dive pulse drops https://www.medtechdive.com/news/fda-starts-510k-pilot-to-cut-optical-tomography-processing-times/540445/ FDA starts 510(k) pilot to cut optical tomography processing times | MedTech Dive The program aims to give developers of optical coherence tomography devices the chance to discuss premarket performance testing recommendations with the agency. 510 k processing times medtech dive fda starts https://www.fda.gov/medical-devices/device-approvals-and-clearances/510k-clearances 510(k) Clearances | FDA Listings of CDRH Substantially Equivalent 510(k)s are normally available about the 5th of each month for the prior month. 510 k clearances fda