Guard Medical Announces FDA 510(k) Clearance for Additional Large Sizes of Its Novel NPseal® NPWT Surgical Dressingnews2024-08-19T15:19:44+00:00August 19th, 2024|Medical Device News Magazine|
Pneuma Systems Infusion Technology Accepted by FDA’s Highly Selective Safer Technologies Program (STeP)news2024-08-12T12:41:01+00:00August 12th, 2024|Medical Device News Magazine|
Labcorp Receives FDA De Novo Marketing Authorization for PGDx elio plasma focus Dxnews2024-08-02T13:39:32+00:00August 2nd, 2024|Medical Device News Magazine|
FDA Approves First Gene Therapy to Treat Adults with Metastatic Synovial Sarcomanews2024-08-02T13:32:53+00:00August 2nd, 2024|Medical Device News Magazine|
Stryker’s Spine Guidance 5 Software featuring Copilot receives 510(k) clearance from FDAnews2024-07-30T14:56:04+00:00July 30th, 2024|Medical Device News Magazine|
Asensus Surgical Receives FDA 510(k) Clearance for Senhance Surgical System in Urologynews2024-07-23T11:14:22+00:00July 23rd, 2024|Medical Device News Magazine|
Spryte Medical Receives Breakthrough Device Designation from FDA for Revolutionary neuro Optical Coherence Tomography (nOCT) Technologynews2024-07-22T14:01:35+00:00July 22nd, 2024|Medical Device News Magazine|
eCential Robotics Receives FDA 510(k) Clearance for Spine Navigation and Robotic-Assistance Devicenews2024-07-22T12:49:40+00:00July 22nd, 2024|Medical Device News Magazine|
FDA Approves Roche’s Vabysmo Prefilled Syringe for 3 Leading Causes of Vision Lossnews2024-07-05T08:06:27+00:00July 5th, 2024|Medical Device News Magazine|
Nyxoah Submits Fourth and Final Module in PMA Application for Genio to the US FDAnews2024-07-01T06:56:09+00:00July 1st, 2024|Medical Device News Magazine|
