The US Food and Drug Administration (FDA) has cleared Miach Orthopaedics Bridge-Enhanced ACL Restoration (BEAR) implant for ...

Sooma Medical has received the approval of an investigational device exemption (IDE) from the US Food and Drug Administration ...

Australia’s Therapeutic Goods Administration (TGA) has approved Body Vision Medical’s AI-powered advanced imaging system, ...

Neuromod Devices has secured €10m ($10.8m) in equity financing to broaden the reach of Lenire, its treatment device.

Oral hygiene is driving the demand for restorative and preventative solutions in the dental market and even outside of dental ...

The US Food and Drug Administration (FDA) has given the greenlight to Caristo Diagnostics for CaRi-Plaque, an artificial ...

Dexcom was issued with an FDA warning letter after issues with “manufacturing processes and quality management systems.” ...

As momentum continues to build, medical device companies are ramping up their investment in 3D printing technology. Driven by ...

The US Food and Drug Administration (FDA) has granted 510(k) clearance to Beckman Coulter Diagnostics' new DxC 500i Clinical ...

Shoulder Innovations has secured $40m in a Series E equity financing round, to mainly progress the commercialisation of ...

Merit Medical has enrolled the first patient in the PREEMIE study of the Bloom Micro Occluder System, aimed at treating PDA.

The US Food and Drug Administration (FDA) has granted 510(k) clearance to Zimmer Biomet's Persona Revision SoluTion Femur.