The regulatory nod in Japan further expands the reach of Medtronic system, already approved to treat AFib in the U.S., Europe ...

The FDA said that Megadyne initiated a voluntary recall of its Mega Soft pediatric patient return electrodes, discontinuing the product.

Retriever Medical is on the hunt for investors to fund continued development and FDA 510(k) clearance of its unique ...

OrthoXel announced that it received FDA 510(k) clearance for its Vertex hip fracture nail (HFN) for fracture fixation.

Nevro (NYSE:NVRO) announced that it appointed Christofer Christoforou as its new chief operating officer, effective May 15.

Acutus Medical has been delisted from the Nasdaq Capital Market, according a recent filing with the U.S. Securities and ...

Neuralink's brain-computer interface Link has encountered its first problem in its first human patient, the company reported.

Steris, a major provider of sterilization products and services, announced a targeted restructuring to prepare for future ...

R3 Vascular announced today that it closed an $87 million Series B financing round and appointed Christopher Owens as ...

Pulse Biosciences (Nasdaq:PLSE) today announced the first U.S. procedure with its CellFX nsPFA percutaneous electrode system.

The FDA shared "continued safety and quality concerns" about Getinge/Maquet cardiovascular recalls as MDRs continue despite ...

Outset Medical (Nasdaq: OM) shares fell this morning on first-quarter misses and restructuring resulting in headcount ...