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New York treating a patient for dry eye using Tixel i®.

Rapid Growth Welcomed as Leading New York Ophthalmologist Integrates Tixel® into Dry Eye Treatments

Dr. Noaman Sanni, a leading ophthalmologist and CEO of Center for Sight New York, has witnessed significant patient and revenue growth after adding Tixel i into his practice. Tixel i, Novoxel's FDA-cleared device, utilizes patented Thermo-Mechanical Action® (TMA) to effectively treat Meibomian Gland Dysfunction (MGD) – a common cause of dry eye – in under two minutes.

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West Plano Dry Eye

Sustained Dry Eye Relief Achieved with Tixel® Treatment

A new article in JOJ Ophthalmology confirms Tixel i® provides sustained, strong clinical outcomes for patients with Evaporative Dry Eye Disease (DED) caused by Meibomian Gland Dysfunction (MGD). This FDA-cleared, non-invasive device uses patented Thermo-Mechanical Action® (TMA®) to deliver durable improvements in key indicators, including patient satisfaction and clinical results.

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ZEISS INTRABEAM 700

ZEISS Gains FDA Approval for INTRABEAM 700, Advancing Intraoperative Radiotherapy Solutions

As a leading provider of medical solutions in the field of neurosurgery, ZEISS Medical Technology is also dedicated to shaping modern oncology. The company recently received 510(k) clearance from the US Food and Drug Administration (FDA) for INTRABEAM® 700 – a leading-edge platform that provides robotic-assisted precision to support intraoperative radiation therapy (IORT).

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VAS-101 in TopiClick dispenser.

In the United States, Vascarta commences Phase 1 clinical study of VAS-101 for sickle cell disease as part of the Proof of Concept

A first in human proof of concept phase I clinical study of VAS-101 (Vasceptor®; topical curcumin gel) in sickle cell disease (SCD) is underway. The study is being conducted by the Foundation for Sickle Cell Disease Research (FSCDR) in Hollywood, Florida, under the supervision of the principal investigator, Dr. Gershwin Blyden.

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RS001 Cardio-respiratory

Respiree secures Singapore HSA clearance for its pediatric expansion of the cardio-respiratory wearable and its new EHR streamlined platform

AI/ML health tech startup Respiree has received clearance from the Health Sciences Authority (HSA) to extend its RS001 cardio-respiratory wearable to pediatric populations. This clearance also enables the extension of Respiree's software platform, introducing enterprise-grade pathway management services and EHR interoperability which further enhances its innovative healthcare solutions.

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