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December 4, 2025
THE LATEST ON THE MEDICAL DEVICE INDUSTRY
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Reducing Ethylene Residuals: Five Steps Developers Can Take

 
Reducing Ethylene Residuals: Five Steps Developers Can Take

Since EO is still a primary sterilization option for many medical device manufacturers, it’s important for them to be sure they address challenges such as residuals.
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Stryker Promotes 27-Year Veteran Spencer Stiles to President, COO

Stiles began his career with Stryker’s Endoscopy business in 1999.

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Providence Enterprise is a Hong Kong Medical Device Contract Manufacturer

Class I and II medical devices with manufacturing in China & Vietnam. We specialize in electro-mechanical assemblies and high-volume disposables.

OEM News

Medtronic Wins FDA Nod for Hugo Surgical Robot in Urologic Procedures

Hugo was cleared for use in minimally invasive urologic surgical procedures including prostatectomy, nephrectomy, and cystectomy.

OEM News

FDA OKs Algorithm Updates to Insulet’s Omnipod 5 Insulin Pump

The updates set a new benchmark in tubeless diabetes technology by providing a lower 100 mg/dL Target Glucose option

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Optimizing Extrusion to Meet Medtech’s Tubing Needs—An MPO Videobites

Dave Kramer of DuPont explains what the company is doing to better serve its tubing customers and how it differentiates itself against competitors.

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OEM News

GE HealthCare, URMC Ink 7-Year Care Alliance Deal

The duo aims to implement efficiencies across the system that can help to decrease burdens on IT, biomed, and clinicians.

OEM News

RSNA 2025: Siemens Healthineers Advances Coronary Artery Disease Management

New software solution supports clinical decision-making by quantifying and qualifying plaque burden.

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Catch Up on MPO Summit 2025 – Now Available On Demand!

The Summit simultaneously highlighted the appeal of the region for medtech while tackling a number of the most significant issues for today’s medical device companies.

OEM News

Getinge, SteriPro International Team Up for Sterile Processing Optimization

The pair intend to raise quality, increase transparency, and steer meaningful cost efficiencies for healthcare facilities.

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Avoiding Additive Manufacturing Deficiencies in Premarket Submissions to FDA

Some key players in the fight include additive manufacturers or regulatory specialists experienced in additive manufactured device submissions.

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Solution Center SPOTLIGHT

Qosina

For nearly 45 years, Qosina has been a trusted partner to medical device engineers, providing thousands of in-stock components and innovative solutions to meet the industry’s evolving needs. Qosina delivers high-quality components and practical support. Serving diverse applications, Qosina’s extensive product portfolio includes over 5,000 components across 25+ categories. With same-day shipping, flexible order quantities, and an ISO 8 Class 100,000 cleanroom for repackaging, Qosina ensures timely, customized solutions that meet your project’s unique demands. Whether you’re in the design or development phase, Qosina is here to support you with practical, reliable solutions at every step. Log on to qosina.com today to see our full product offering.