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MedTech Economics

December 13, 2016
Ameing for Asia

Be Very Careful in China’s Medical Device Market

By Ames Gross

Don’t skimp on conducting due diligence.

Continue reading →

November 28, 2016

Eye Care Needs Rising Quickly in Asia

By Ames Gross

A lack of quality, locally made products opens the door for Western device companies.

Continue reading →

November 21, 2016

Integrated, Digital Devices Among Top Technologies at MEDICA 2016

By Maria Fontanazza

This year’s event highlighted the continuing global shift in healthcare to smarter technologies that leverage data and improve decision making.

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November 17, 2016

How to Evaluate Attractiveness of Product Ideas and Markets Before Development

By Karl-Hubertus Gruber, Michael Marquardt, Ph.D., Laszlo Horwitz

Conducting pre-analysis prior to taking on the risk of costly development can help medtech companies avoid failure.

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Medtech, innovation
October 31, 2016
Medtech, innovation

Keeping Patients in Mind: Demand for Digitization

By Dr. Lutz Retzlaff

MEDICA Health IT Forum addresses workable solutions for device companies.

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American Flag
October 28, 2016
American Flag

MedTech and the 2016 Election: Who Wins?

By Maria Fontanazza

The candidates have said little about what they will do for the medical device industry.

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Boston Scientific
October 27, 2016
Boston Scientific

Boston Scientific Hits $2.1 Billion in Q3 Sales

By MedTech Intelligence Staff

The company is performing well across all business units and geographies.

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Medtronic
October 26, 2016
Medtronic

Medtronic Wins FDA Approval for Largest TAVR System in United States

By MedTech Intelligence Staff

The device expands treatment to an additional patient population.

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ASEAN, Southeast Asia
October 25, 2016
ASEAN, Southeast Asia

Skyrocketing Healthcare Demand in ASEAN Opens Door to Medtech

By Ames Gross

Foreign device companies can expect a big opportunity for expansion in Southeast Asia.

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October 18, 2016

Global Revenue Drops, MedTech Struggle for Growth Signals Industry Shift

By Maria Fontanazza

Ernst & Young’s annual Pulse of the Industry report reveals decreasing global revenue and financing in the medtech industry.

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Columns

March 27, 2026

Artificial Intelligence: ROI, not Clinical Autonomy, Leads Operational Workflows

By MedTech Intelligence Staff

What we’re reading on LinkedIn… Review of leading healthcare AI reports illustrate several conditions creating fertile ground for applied AI in healthcare operations.

March 20, 2026

Mindray North America Enters Ventilator Market

By MedTech Intelligence Staff

Mindray says its entry into the ventilator market marks a significant step in expanding advanced respiratory care options for clinicians and patients, reinforcing the medical device leader’s commitment to driving innovation in healthcare.

March 20, 2026

LivaNova Receives FDA Premarket Approval for to treat Moderate to Severe Obstructive Sleep Apnea

By MedTech Intelligence Staff

Hypoglossal nerve stimulation therapy approved in the U.S. without complete concentric collapse contraindication or warning language. The next-generation, MRI-compatible device is expected to launch in the first half of 2027, pending FDA supplement review.

March 20, 2026

EPA proposes new rule on Ethylene Oxide Emissions: Could Loosen Limits on Medical Device Sterilization

By MedTech Intelligence Staff
EPA Logo

The medical device industry and EPA have been in ongoing debate over balancing the need for sterile medical equipment with concerns about pollution near sterilization plants.

March 18, 2026

Prodeon Medical FDA 510(k) approved for the Urocross Expander System, a Non-Permanent Retrievable Implant for Treating Benign Prostatic Hyperplasia

Prodeon Medical

The Urocross Expander System is designed to remodel the obstructing prostatic lobes during the six-month indwell time and is intentionally retrieved, leaving no permanent foreign material behind.

March 18, 2026

JenaValve Gets FDA Nod for Trilogy Transcatheter Heart Valve (THV) to Treat Aortic Regurgitation (ssAR)

By MedTech Intelligence Staff
JenaValve

With its FDA approval, JenaValve intends to commence launch activity for the Trilogy System immediately with participating clinical study sites.

March 5, 2026

RadNet Acquires Gleamer to Support Position as a Radiology Clinical AI Solutions Leader

RadNet leadership says the acquisition of Biocare enhances Agilent’s pathology portfolio and reflects our strategy to drive long-term growth through customer-centric innovation and disciplined capital allocation.

February 26, 2026

FDA Approval for BIOTRONIK Solia CSP S Pacing Lead For LBBAP

By MedTech Intelligence Staff
Biotronik logo

Biotronik has received U.S. Food and Drug Administration (FDA) approval for its Solia CSP S pacing lead, growing access to a solution for Left Bundle Branch Area Pacing (LBBAP).

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