FDA Denies Marketing of Logic’s Menthol E-Cigarette Products Following Determination They Do Not Meet Public Health Standardnews2022-10-26T19:20:18+00:00October 26th, 2022|Medical Device News Magazine|
NeuroOne® Receives FDA 510(k) Clearance to Market its Evo® sEEG System for Less than 30 Day Usenews2022-10-25T13:18:50+00:00October 25th, 2022|Medical Device News Magazine|
MedAlliance SELUTION SLR Receives Coronary FDA IDE Approvalnews2022-10-24T14:36:01+00:00October 24th, 2022|Medical Device News Magazine|
Sol-Millennium Receives FDA Clearance for Sol-Guard Safety Pull Button Blood Collection Setnews2022-10-19T17:40:55+00:00October 19th, 2022|Medical Device News Magazine|
Medtronic First to Receive FDA Approval for Pacing the Heart’s Natural Conduction Systemnews2022-10-17T13:15:48+00:00October 17th, 2022|Medical Device News Magazine|
XACT Robotics ® Receives FDA Clearance for its ACE Xtend™ Remote Control Unitnews2022-10-11T19:12:21+00:00October 11th, 2022|Medical Device News Magazine|
New FDA Draft Guidance Aims to Protect Children who Participate in Clinical Trialsnews2022-09-23T15:31:14+00:00September 23rd, 2022|Medical Device News Magazine|
iMediSync Announces ‘iSyncWave’ EEG Scanner Receives FDA 510k clearancenews2022-09-23T12:14:36+00:00September 23rd, 2022|Medical Device News Magazine|
Zimmer Biomet Receives FDA Clearance for Identity Shoulder System for Shoulder Replacementnews2022-09-20T11:19:46+00:00September 20th, 2022|Medical Device News Magazine|
ABK Biomedical Receives FDA 510(k) Clearance of Easi-Vue Embolic Microspheresnews2022-09-12T16:15:17+00:00September 12th, 2022|Medical Device News Magazine|
