Boston Scientific Receives FDA Approval for Expanded Labeling of WATCHMAN FLX LAAC Device for Dual Anti-Platelet Therapy as Post-Procedural Medication Optionnews2022-09-06T12:26:26+00:00September 6th, 2022|Medical Device News Magazine|
Insulet Announces FDA Clearance of Omnipod 5 for Children Aged Two Years and Older with Type 1 Diabetesnews2022-08-22T12:50:12+00:00August 22nd, 2022|Medical Device News Magazine|
Zavation Medical Products, LLC, receives FDA 510K Clearance for Varisync Anterior Cervical Plate and Spacer System As An Addition to its Cervical Spine Portfolionews2022-08-18T14:51:09+00:00August 18th, 2022|Medical Device News Magazine|
CerroZone Receives FDA 510(k) Class II Clearancenews2022-08-15T19:14:04+00:00August 15th, 2022|Medical Device News Magazine|
Dyad Medical Secures FDA Clearance For Echo:Prio ™ Cardiac Imaging Analysis Platformnews2022-08-15T19:07:47+00:00August 15th, 2022|Medical Device News Magazine|
Avenda Health Receives FDA Investigational Device Exemption for AI-enabled Prostate Cancer Therapynews2022-08-09T14:53:50+00:00August 9th, 2022|Medical Device News Magazine|
MedAlliance SELUTION SLR Receives Second FDA IDE Approvalnews2022-08-09T14:38:14+00:00August 9th, 2022|Medical Device News Magazine|
Movano Ring Exceeds Accuracy Targets for SpO2 and Heart Rate Monitoring in Initial Hypoxia Study; Company Eyes FDA Submissionnews2022-08-09T14:30:39+00:00August 9th, 2022|Medical Device News Magazine|
NeuroOne Submits Special 510(k) to FDA for Evo® sEEG Electrodenews2022-08-09T14:21:02+00:00August 9th, 2022|Medical Device News Magazine|
MicroPort Navibot Receives 510(K) Clearance for SkyWalker™, the Company’s First Robot-Assisted Platform for Orthopedic ApplicationsInews2022-08-09T11:02:51+00:00August 9th, 2022|Medical Device News Magazine|
