Category: Uncategorized

Volition Demonstrates Utility of Rapid, Point-of-Care Finger-Prick Test in Sepsis Patients

August 12, 2026

HENDERSON, Nev., Aug. 12, 2026 /PRNewswire/ — VolitionRx Limited (NYSE AMERICAN: VNRX) (“Volition”), a multi-national epigenetics company, today announces that results utilizing its lateral flow prototype are highly correlated with results utilizing Volition’s established automated Nu.Q® NETs test in critically ill sepsis patients1 , thereby expanding beyond centralized laboratory testing.

Wandercraft wins FDA clearance for self-balancing exoskeleton

August 12, 2026

Wandercraft, a Paris-based robotics company, announced that the FDA has granted clearance for Eve, its personal self-balancing exoskeleton designed to support upright mobility.

Datasea Announces FDA Registration and Device Listing for NeuroVibe Acoustic BCI Biofeedback System as a Class II 510(k)-Exempt Biofeedback Medical Device

August 11, 2026

BEIJING, Aug. 11, 2026 /PRNewswire/ — Datasea Intelligent Technology Ltd. (NASDAQ: DTSS) (“Datasea” or the “Company”), a technology company focused on acoustic high-tech and AI multimodal digital solutions, today announced that Shuhai Jingwei (Shenzhen) Information Technology Co., Ltd. (“Shuhai Jingwei”), the Company’s variable interest entity in China, has completed establishment registration and device listing with the U.S. Food and Drug Administration (“FDA”) for its NeuroVibe Biofeedback System, including products NV-02 and NV-03.

BlueWind Medical lands FDA clearance for UUI implant with 15-year lifespan

August 6, 2026

BlueWind plans to initiate a limited US market launch of Revi Extend in Q4 2026.

Common blood storage bags may leach microplastics into stored blood

August 6, 2026

In the 1970s, PVC bags revolutionized the storage of blood and blood products for transfusion. Disposable plastic (PVC) bags replaced reusable glass bottles, making the process more convenient and safer from contamination. Over half a century later, the same disposable plastic bags are creating a new kind of problem because of microplastics (MPs). These tiny particles, less than 5 millimeters in size, are formed by the polymer degradation of plastic materials as they break down and age.

Koning Health Achieves MDSAP Certification

August 4, 2026

Certification strengthens Koning’s global regulatory foundation as two new Vera Breast CT systems expand patient access in key U.S. markets

What to know about the record-setting Cyclospora outbreak

July 21, 2026

Two Northwestern experts explain how to reduce risk without sacrificing a healthy diet

HoneyNaps Receives U.S. FDA 510(k) Clearance for SOMNUM V3.0 for AI-Based Sleep-Disordered Breathing Analysis

July 16, 2026

BOSTON, July 16, 2026 /PRNewswire/ — HoneyNaps, an AI-based sleep medicine company, today announced that SOMNUM V3.0, its AI diagnosis software for polysomnography (PSG) analysis, has received U.S. Food and Drug Administration (FDA) clearance under clearance number K253390.

ElectroWire Medical gains FDA clearance for transseptal puncture system

July 16, 2026

The LightningWire system is designed to support transseptal access in procedures such as atrial fibrillation ablation, left atrial appendage closure and transcatheter mitral interventions.

Simple Urine Test Could Transform Early Detection of Chronic Kidney Disease, Lancet Series Finds

July 16, 2026

The disease is projected to become the fifth leading cause of death by 2040 if diagnosis and treatment rates do not improve

Blog

- Uncategorized

Volition Demonstrates Utility of Rapid, Point-of-Care Finger-Prick Test in Sepsis Patients

Wandercraft wins FDA clearance for self-balancing exoskeleton

Datasea Announces FDA Registration and Device Listing for NeuroVibe Acoustic BCI Biofeedback System as a Class II 510(k)-Exempt Biofeedback Medical Device

BlueWind Medical lands FDA clearance for UUI implant with 15-year lifespan

Common blood storage bags may leach microplastics into stored blood

Koning Health Achieves MDSAP Certification

What to know about the record-setting Cyclospora outbreak

HoneyNaps Receives U.S. FDA 510(k) Clearance for SOMNUM V3.0 for AI-Based Sleep-Disordered Breathing Analysis

ElectroWire Medical gains FDA clearance for transseptal puncture system

Simple Urine Test Could Transform Early Detection of Chronic Kidney Disease, Lancet Series Finds