VUZE Medical Announces U.S. FDA 510(k) Clearance for Its VUZE Systemnews2022-01-18T17:14:16+00:00January 18th, 2022|Medical Device News Magazine|
FDA Approves Cochlear Nucleus Implants for Unilateral Hearing Loss/single-sided Deafnessnews2022-01-11T16:54:06+00:00January 11th, 2022|Medical Device News Magazine|
Lazurite™ Announces FDA 510(k) Submission for its ArthroFree™ Wireless Camera Systemnews2022-01-11T16:15:01+00:00January 11th, 2022|Medical Device News Magazine|
FDA Pre-Submission Filed for Cardio inCode-SCOREnews2022-01-11T13:46:27+00:00January 11th, 2022|Medical Device News Magazine|
BD Introduces Smart Connected Robotics to Automate Microbial Identification (BD Kiestra™)news2022-01-07T13:16:03+00:00January 7th, 2022|Medical Device News Magazine|
VySpine Announces FDA Clearance of the VySpan PCT Systemnews2022-01-06T21:06:43+00:00January 6th, 2022|Medical Device News Magazine|
BIOLASE and EdgeEndo Announce FDA 510(k) Clearance of New EdgePRO Laser-Assisted Microfluidic Irrigation Device for Endodontistsnews2022-01-06T15:16:41+00:00January 6th, 2022|Medical Device News Magazine|
Endotronix Announces FDA Approval for PROACTIVE-HF Pivotal Trial Design Change to Single-Arm Studynews2022-01-05T17:14:51+00:00January 5th, 2022|Medical Device News Magazine|
NuVasive Receives FDA Clearance for Expanded Indications of Use for Attrax Putty with Company’s Thoracolumbar Interbody Portfolionews2022-01-05T12:31:57+00:00January 5th, 2022|Medical Device News Magazine|
Zynex Submits FDA Application for its Next Generation Fluid and Blood Volume Monitornews2022-01-03T14:41:52+00:00January 3rd, 2022|Medical Device News Magazine, Uncategorized|
