Social Media Ideas for Medical Devices

FDA Medical Devices: Important Regulatory Considerations for Companies Seeking to Enter the U.S. Market

The medical device market in the U.S. is very large and attractive to many companies who are located outside of the U.S. Entering the U.S. medical device market requires a comprehe...

Advancing Care Through Cardio & Vascular Device Development Services

Key Takeaways Cardiovascular devices operate in one of the most demanding areas of healthcare. A... The post Advancing Care Through Cardio & Vascular Device Development Service...

Patient-centered device design is not bedside manner

This year I interned at Dr. Ziauddin Hospital during my biomedical engineering studies. Much of what I learned there was not to be found in books. At the moment it was standing nex...

FDA chief Tukaram flags huge price gaps in medical devices, seeks Centre’s intervention

The report cited that an IV set purchased for ₹11.05 had a declared MRP of ₹325, while an infusion set purchased for ₹11 had an MRP of ₹201.

NPPA’s limited powers pose hurdle to 20% cap on medical device margins

Under the Drugs (Prices Control) Order, 2013 (DPCO), NPPA can directly fix prices only for “scheduled” drugs and devices

Dutch Medical Device Maker, Medical Precision, Enters U.S. Market With FDA-Cleared Comfort Marker

Radiotherapy patient-marking device, engineered with technology from the permanent make-up industry, will make its U.S. clinical debut at…

Small Components, Big Impact: How Batteries, Frequency Control Products, and RTC Modules Enable Modern Diagnostic and Th...

Portable medical technology is increasingly becoming an integral part of patients’ everyday lives. Modern diagnostic and therapeutic devices enable continuous health monitoring and...

Nutromics Nabs FDA Breakthrough Status for Antibiotic Monitoring Patch

Nutromics earned FDA breakthrough device designation for its wearable patch that tracks vancomycin levels in real time. The device aims to replace the periodic blood draws currentl...

This Device Could Prevent Lung Biopsy’s Most Common — and Costly — Complication

Selio Medical developed an FDA-cleared hydrogel device that seals CT-guided lung biopsy punctures before they can cause pneumothorax — a collapsed lung complication that affects up...

What Does 'Medical Grade' Mean? 5 Things To Check Before You Buy A Device

The phrase "medical grade" suggests that a product meets high standards of quality or performance. However, its meaning depends on the product, the claims being made and the applic...

Biomaterials and Biofabrication Push Medical Implants Toward Multifunctional Devices

Medical implants are no longer passive pieces of hardware. A titanium screw or an artificial hip must do far more than provide mechanical support or stand in for damaged tissue: it...

Royal Sandur Group company forays into medical devices and consumables

A long-term lease deed was executed between Royal Sandur MedTech Private Limited and Andhra Pradesh MedTech Zone Limited for setting up a manufacturing unit

Laser Marking Technologies, LLC Announces FDA-Compliant UDI Marking Solutions for Medical Device Manufacturers Navigatin...

A new FDA inspection standard is making Unique Device Identification marking accuracy an actively enforced requirement, and Laser Marking Technologies, LLC offers cost-conscious la...

Advanced Joining and Laser Processing Solutions for Medical Device Manufacturing

Advanced Joining and Laser Processing Solutions for Medical Device Manufacturing Booth 2921 at MD&M Midwest exhibition in Minneapolis, Oct. 28–29, 2026 Quali...

Virtual e-health system VIRTUES shows overwhelmingly positive results for monitoring cardiac devices

The End of the Waiting Room? Virtual Monitoring of Pacemakers and Defibrillators Proves as Safe as Clinic Visits — and Cheaper Every year, roughly 1.25 million people worldwide hav...

Why FDA Clearance Alone Can’t Guarantee Medical Device Success

Why FDA Clearance Alone Can’t Guarantee Medical Device Success Anonymous (not verified) Thu, 10/15/2026 - 10:12 pharmagather item url Why FDA Clearance Alo...

Lifesaving Lincoln Laboratory device wins 2026 Excellence in Technology Transfer Award

The handheld catheterization device AI-GUIDE, created by Lincoln Laboratory and Massachusetts General Hospital, promises improved health outcomes for injured service members and c...

Are Hospital Operating Rooms Ready For FDA’s Expectations for Surgical Robots?

The FDA recently published draft guidance on pre-market testing for robotically-assisted surgical devices, raising timely discussion around whether hospital infrastructures are cap...

Wireless Power Keeps Implants Running

A new wearable-to-implant wireless power system maintains energy delivery despite movement, stretching, and misalignment, potentially enabling battery-free soft medical implants fo...

The Medical Device Launch Playbook: Patents, FDA, Reimbursement and Strategic Timing

Bringing a medical device to market requires companies to navigate patent protection, FDA requirements, reimbursement, quality systems and commercialization planning, often at the...

Implanted sensor could detect worsening heart failure before symptoms appear

A tiny implanted sensor being evaluated in an international clinical trial could give physicians an earlier warning that a patient’s heart failure is worsening — potentially before...

Generative AI Is Coming to Medical Devices. FDA Is Already Thinking About What Comes Next.

Trimedx Agentic AI Capabilities Reduce Medical Device Cybersecurity Remediation

Trimedx Agentic AI Capabilities Reduce Medical Device Cybersecurity Remediation Delivering up to 95% identification and matching accuracy for connected medical devices...

Renewal Season is Here! FY 2027 Device Establishment Registration and Listing

By Steven J. Gonzalez —