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Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Dec. 1, 2021

View Archived Issues
Group of kids, faces huddled together

Memed posts positive data from pediatric clinical trial evaluating infection test

Memed Diagnostics Ltd. has published new data from an EU Commission funded clinical trial evaluating its blood test for differentiating bacterial and viral infections. The prospective, multicenter cohort study, titled “AutoPilot-Dx,” was carried out in emergency wards in Italy and Germany. The goals of the study were to validate the performance of Memed’s BV test in a broad pediatric population with respiratory tract infections or fever without source and estimate its potential to impact antibiotic use. Read More
Illustration of intestines overlayed on human torso

Metame receives FDA clearance for IBS digital therapy

The FDA granted 510(k) clearance to Metame Health Inc.’s Regulora, the company’s prescription digital therapeutic (PDT) for abdominal pain associated with irritable bowel syndrome (IBS). Regulora provides gut-directed hypnotherapy in a smartphone app that is designed to help patients better manage their symptoms and address miscommunication between the brain and gut that contributes to sensations of pain. Read More
Regulatory-US-FDA-HQ.png

Complaint handling, CAPA a common theme in two new FDA warning letters

Device makers have historically struggled to maintain adequate procedures for corrective and preventive action (CAPA) and complaint handling (CH), and two warning letters posted to the FDA website suggest these are still sore spots. Invacare Corp., of Elyria, Ohio, and Smiths Medical ASD Inc., of Minneapolis, were both cited for CAPA and CH deficiencies. Read More
Cancer cells under magnifying glass

Canada approves Koios’s AI-driven, breast cancer ultrasound software

TORONTO – Koios Medical Inc. has received Health Canada approval for its DS Smart Ultrasound decision support software, which the company said accurately interprets breast ultrasound examinations. Company CEO Chad McClennan told BioWorld greater accuracy will provide early cancer detection rates, while reducing costly false positives and unnecessary biopsies. Read More
FDA-yellow-dice.png

FDA slots five device types into class II, including for de novo granted in 2011

The FDA’s device center is required to develop and publish special controls for devices that are deemed class II items via the de novo petition process, and five such declarations were posted Dec. 1 to the Federal Register. One of these de novo classifications, for conditioning tools for eating disorders, was the subject of a de novo petition filed in 2007 and granted in 2011. Read More

Appointments and advancements for Dec. 1, 2021

New hires and promotions in the med-tech industry, including: Biosig, Healthy.io, Invacare, Kheiron Medical, Pacbio, Paragon 28. Read More

Financings for Dec. 1, 2021

Med-tech firms raising money in public or private financings, including: Aditxt. Read More

In the clinic for Dec. 1, 2021

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Angle, Memed, Seno. Read More

Other news to note for Dec. 1, 2021

Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Alio, Ambu, Biodesix, Bolder Surgical, Canon Medical, Concertai, Darvis, Deepc, Eurofins, Hologic, Includehealth, Labcorp, Lifeline Vascular Care, London Medical, Mattioli Engineering Italia, Medxhealth, Neo Q, Resoundant, Sensus Healthcare, Spensana, Surgio Health, Vizient. Read More

Regulatory actions for Dec. 1, 2021

Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Directed Systems, Invo Bioscience, Immersivetouch, Reflexion. Read More

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