RANCHO CUCAMONGA, Calif., Oct. 6, 2026 /PRNewswire/ — New World Medical is pleased to announce the Ahmed® Glaucoma Valve (AGV), Ahmed ClearPath® (ACP), and KDB GLIDE® have received Medical Device Regulation (MDR) certification in the European Union.
Combination of Hēlo Thrombectomy System and Hēlo Return establish the first 510(k)-cleared platform compatible with continuous vacuum aspiration
Shenzhen, China, Oct. 10, 2026 /PRNewswire/ — Shenzhen Ninenovo Technology Limited, the parent company of RingConn, announced that its Smart Ring has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for non-invasive blood oxygen (SpO2) measurement (Clearance No. K260490).
A patch the size of a Band-Aid, stuck to your forehead, can now do something no traditional sleep study or fitness tracker can: nudge your brain toward a better night’s sleep. William Coon, a sleep scientist at the Johns Hopkins Applied Physics Laboratory, has built a wearable device, meant to be used at home, that listens to brain activity and uses neurostimulation and other techniques to manufacture deep, restorative sleep.
Sonorous’ FDA IDE approval follows its BosSTENT’s receipt of FDA breakthrough device designation in February 2026.
BridgeSource Medical obtained de novo clearance from the FDA for its handheld cardiac implant identifier, designed to help emergency department clinicians quickly identify a patient’s hardware brand.
A team has developed a new self-disinfecting cotton fabric capable of eliminating bacteria, fungi and viruses in hospital settings using visible light.
CAMBRIDGE, England, Oct. 6, 2026 /PRNewswire/ — Cambridge Heartwear® Limited (www.camheartwear.com) has secured a landmark £184 million tender with the National Health Service (NHS) of the UK for HeartSense®, the world’s first medical-grade, multi-channel, portable, wirelessly charged ECG wearable straight to one’s mobile phone, representing a significant advancement in global Medical technology, AI application and cardiovascular diagnostics.
Happy Health’s Happy Ring previously secured FDA approval for its use in the diagnosis and monitoring of sleep apnoea.
The Class II decision-support software analyses lung sound recordings from compatible FDA-cleared electronic stethoscopes and flags recordings suggestive of wheeze for clinical review.