Latest News

Intact Vascular completes enrollment in TOBA II trial of Tack Endovascular system

Medical device firm Intact Vascular has closed enrollment in the tack optimised balloon angioplasty II (TOBA II) clinical trial of its Tack Endovascular system to treat patients with...

Intact Vascular completes enrollment in TOBA II trial of Tack Endovascular system

Zoll's new AED models get Health Canada approval

Zoll's new AED models get Health Canada approval

Origin begins treatment in Phase IIb-equivalent trial of NO technology to treat DFUs

US-based medical technology firm Origin has started treating patients in the Phase IIb-equivalent GENESIS trial of its nitric oxide (NO) technology for the treatment of chronic diabetic foot...

Origin begins treatment in Phase IIb-equivalent trial of NO technology to treat DFUs

Abbott reports positive one-year outcomes from study of MitraClip for TMVR in US

Healthcare company Abbott has reported positive one-year outcomes from a real-world study of the use of its MitraClip system in transcatheter mitral valve repair (TMVR) procedures in the...

Abbott reports positive one-year outcomes from study of MitraClip for TMVR in US

Centurion introduces new radial arterial catheterisation kit

Centurion introduces new radial arterial catheterisation kit

Medtronic obtains FDA approval for Melody transcatheter pulmonary valve

Medtronic obtains FDA approval for Melody transcatheter pulmonary valve

Teleflex secures 510(k) clearance for Spectre guidewire and Torque dual access catheter

Medical technologies provider Teleflex has secured 510(k) clearance from the Food and Drug Administration (FDA) for its Spectre guidewire and Torque dual access...

Teleflex secures 510(k) clearance for Spectre guidewire and Torque dual access catheter

Spineology's interbody fusion system receives expanded FDA clearance

Spineology's interbody fusion system receives expanded FDA clearance

PQ Bypass's DETOUR percutaneous technologies secure CE mark

US-based medical device company PQ Bypass has secured CE mark approval for its DETOUR percutaneous bypass technologies TORUS stent graft system, PQ Snare and PQ Crossing...

PQ Bypass's DETOUR percutaneous technologies secure CE mark

Medtronic commences clinical study of paclitaxel-coated PTA balloon catheter to treat PAD

Medtronic has commenced an IN.PACT BTK clinical study of IN.PACT 0.014 paclitaxel-coated percutaneous transluminal angioplasty (PTA) balloon catheter to treat patients with below-the-knee...

Medtronic commences clinical study of paclitaxel-coated PTA balloon catheter to treat PAD

FDA grants premarket approval to Zoll's new defibrillator

FDA grants premarket approval to Zoll's new defibrillator

ZS Genetics, Hitachi High partner to develop, commercialise new DNA sequencing platform

ZS Genetics has entered into a strategic collaboration with Hitachi High Technologies America (HTA), to develop and commercialise its new single molecule DNA sequencing...

ZS Genetics, Hitachi High partner to develop, commercialise new DNA sequencing platform

Ethicon introduces new energy device for jaw tissue sealing

Ethicon introduces new energy device for jaw tissue sealing

Gore gets Health Canada approval for TIGRIS vascular stent use in PAD

Gore gets Health Canada approval for TIGRIS vascular stent use in PAD

MicroVention's HydroCoil system demonstrates positive outcome in GREAT trial for aneurysm

MicroVention, a US subsidiary of Japan-based medical device firm Terumo, has reported a positive outcome from the GREAT trial of its 2nd generation HydroCoil embolic system coils in the...

MicroVention's HydroCoil system demonstrates positive outcome in GREAT trial for aneurysm

Tryton Medical's side branch stent secures FDA approval for coronary bifurcation lesions

Stent systems developer Tryton Medical has obtained the US Food and Drug Administration (FDA) premarket approval (PMA) for its Tryton Side Branch Stent to treat coronary bifurcation...

Tryton Medical's side branch stent secures FDA approval for coronary bifurcation lesions

Agilent Technologies unveils new CGH assay to detect genetic anomalies

US-based Agilent Technologies has introduced its new comparative genomic hybridisation (CGH) assay for use in diagnostic...

Agilent Technologies unveils new CGH assay to detect genetic anomalies

Keystone Heart, Venus Medtech to offer TAVR + TriGuard combination in Asian markets

Israel-based medical device firm Keystone Heart has entered into a partnership agreement with China-based heart valve developer Venus Medtech (Hangzhou) to offer cerebral embolic protection...

Keystone Heart, Venus Medtech to offer TAVR + TriGuard combination in Asian markets

FDA grants approval to CeloNova's coronary stent system

The US Food and Drug Administration (FDA) has granted regulatory approval to US-based medical device firm CeloNova BioSciences' nanocoated coronary stent system COBRA...

FDA grants approval to CeloNova's coronary stent system

Intersect's new sinus implant receives FDA approval

Intersect's new sinus implant receives FDA approval

Medtronic gets CE mark for CRT pacemakers range

Ireland-based medical technology company Medtronic has obtained CE mark for its range of cardiac resynchronisation therapy pacemakers (CRT-Ps) that enable proactive heart failure...

Medtronic gets CE mark for CRT pacemakers range
cachename:Newscachekey:rd-137342983_-84702732_rd-1665407042_1857678299_rd-488908060_1460672566_ap1460672566_1857678299_-194924008