Onward Medical announced today that the FDA granted breakthrough device designation for its ARC-BCI system that uses brain-computer interface (BCI) technology.
TYLER, Texas–(BUSINESS WIRE)– AIOMEGA, a Texas biomedical company, announced that AIO BREATHE, their medical device that treats Obstructive Sleep Apnea, has been cleared by the Food and Drug Administration.
Nevro1™ Proven to Immediately Transfix Sacroiliac (SI) Joint to Allow for Long-term SI Joint Fusion
Sonus Microsystems has unveiled its latest ultrasound technology, delivering remote diagnostic imaging, without the need to go to a clinic or hospital
TOKYO, Feb. 27, 2024 /PRNewswire/ — PENTAX Medical, a division of HOYA Group, have obtained CE marks for new models of PENTAX Medical i20c Video Endoscope Series – PENTAX Medical Video Colonoscope EC34-i20c, PENTAX Medical Video Upper GI Scope EG27-i20c and R/L Knob Adaptor OE-B17.
Virtual Incision announced that the FDA granted marketing authorization to its MIRA miniaturized surgical robotic system.
The clearance poises the orthopedics company to be first to market with robotic-assisted shoulder replacement surgery.
Allowance for U.S. Patent Application Serial Number 18/107,536 for Tenon’s Catamaran® SI Joint implant for stabilizing a dysfunctional sacroiliac (SI) joint.
For use in children weighing 10 kilograms or more with acute kidney injury (AKI) due to sepsis or a septic condition requiring kidney replacement therapy (KRT).
ClearPoint Neuro (Nasdaq:CLPT) announced that the FDA cleared its ClearPoint 2.2 software with integrated Maestro Brain Modeling.