Pulse Biosciences Receives FDA 510(k) Clearance of Expanded Energy Settings for use with the CellFX® Systemnews2022-08-04T13:01:38+00:00August 4th, 2022|Medical Device News Magazine|
BIOTRONIK Receives FDA Approval of the Pulsar®-18 T3 Peripheral Self-Expanding Stent Systemnews2022-07-26T18:24:43+00:00July 26th, 2022|Medical Device News Magazine|
Radialis PET Imager Receives FDA Clearancenews2022-07-18T17:53:53+00:00July 18th, 2022|Medical Device News Magazine|
Pulnovo Medical Concludes Successfully First Pre-Sub Meeting with FDA for PADN Global Clinical Trialnews2022-07-15T12:42:26+00:00July 15th, 2022|Medical Device News Magazine|
Medtronic Receives FDA Clearance for Next-generation UNiD™ Spine Analyzer with Degenerative Spine Surgery Predictive Modelnews2022-07-14T13:05:54+00:00July 14th, 2022|Medical Device News Magazine|
Mg OSTEOINJECT Receives 510(k) Clearance for Expanded Indicationsnews2022-07-13T19:31:23+00:00July 13th, 2022|Medical Device News Magazine|
FDA Accepts & Closes LimiFlex PMA Modulenews2022-07-13T19:20:20+00:00July 13th, 2022|Medical Device News Magazine|
Renovia Receives FDA Clearance for leva Pelvic Health System as 1st Line RX for Chronic Fecal Incontinencenews2022-07-07T14:57:38+00:00July 7th, 2022|Medical Device News Magazine|
Xoran Technologies Submits FDA 510(k) Application for TRONnews2022-06-30T16:24:22+00:00June 30th, 2022|Medical Device News Magazine|
Renuvion Dermal Handpiece for Wrinkle-Reduction Procedures Cleared by the FDAnews2022-06-28T12:24:24+00:00June 28th, 2022|Medical Device News Magazine|
