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Drop the 'Remote', It's Just Patient Monitoring

Oct 06, 2022

Adding Device Packaging Simulation Testing to Better Achieve Sustainability

Oct 06, 2022

This Week Last Year in Medtech: Oct. 2-8

Oct 06, 2022

Promex Expands its Die Bonding Services & Other Supplier News

Oct 06, 2022

Leading Robotic Surgeon Spills the Tea on Medtronic's Hugo

Oct 06, 2022

Behind the Design: How Dexcom Built a Better CGM

Oct 05, 2022

6 Big Developments Coming Out of TCT 2022

Oct 05, 2022

Quest Strengthens Lab Services Segment with M&A

Oct 05, 2022

U.S. Medtech Incubators and Accelerators

Check out these U.S. medtech incubators and accelerators organized by state.

Highlights

This Week Last Year in Medtech: Oct. 2-8

Oct 06, 2022

See what Boston Scientific and Medtronic were up to this time last year.

Promex Expands its Die Bonding Services & Other Supplier News

Oct 06, 2022

Here’s what was new in the world of medical device suppliers during the week of October 2.

Is HFES a Solution to Reducing Opioid Use & Treating Chronic Pain?

Oct 05, 2022

A recent study showed that high-frequency stimulation inhibits neuroinflammatory mediator release by sensory...

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A Better See-and-Do Technology for Bland Embolization Procedures

Oct 04, 2022

Recently FDA-cleared Easi-Vue embolic microspheres are nondeformable and radiopaque and feature a proprietary delivery system that enables controlled metering of the microspheres into a patient.

Black Women Face Significant Barriers in Obtaining Venture Capital

Oct 03, 2022

A survey-based report by RockHealth suggested that women & black women, who founded medtech companies, have extreme difficulty in obtaining financing from VC firms.

Digital Health Company Epicore Biosystems Won’t Sweat Supply-Chain Bottlenecks

Oct 03, 2022

The maker of sweat-sensing wearables partners with 3M and Innovize to ensure uninterrupted materials supply and production.

FDA User Fee CR Passed, Questions on Policy and Reform Riders Remain

Oct 03, 2022

While a “clean” user fee package has been reauthorized, HR 6833 does not include the FDA policy and reform riders usually included in the “must-pass” bill, leading to many unanswered questions.

careviso Snags $17 Million in Series B Funding

Sep 29, 2022

Its technology platform, seeQer, aims to remove the barriers associated with prior authorizations and financial transparency...

Nordson Opens Mexico Facility & Other Supplier News

Sep 29, 2022

Here’s what was new in the world of medical device suppliers during the week of September 25.

VoxNeuro Partners with Canadian Armed Forces on Concussion Exposure study

Sep 28, 2022

The company will use this information to support regulatory filings with Health Canada and the FDA.

Companion Diagnostic Kit Approved for Support in Gene Therapy Treatment

Sep 28, 2022

Following the EU’s approval of ROCTAVIAN, a gene therapy for severe hemophilia A, ARUP Laboratories, in partnership with BioMarin, has developed the AAV5 DetectCDx kit to help identify patients who are eligible for treatment with the drug.

DURAMESH Suture Receives FDA Nod

Sep 27, 2022

Mesh Suture noted that the aim of DURAMESH is to mitigate the intractable problem of surgical failure due to suture pull-through.

FDA Releases Draft Guidance on Ethics for Pediatric Involvement in Clinical Trials

Sep 26, 2022

The inclusion of children in medical research is important to the development of more effective treatments, however, the ethnics of doing so may raise eyebrows if not careful.

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