Biosurgery in Europe

It appears that the climate is becoming more favorable for surgical sealants and adhesives in Europe, according to "European Markets for New and Emerging Wound Closure Products and Techniques" a report published in April 2007 by Medtech Insight, because health care payers want to bridge the gap between an aging population's high-technological medical product requirements and regional health care cost containment initiatives.

Surgical sealants and adhesives, used to control bleeding and hasten wound closure, have always represented a rather sticky market. Companies with such products always face the difficult challenge of convincing surgeons proud of their skills that these adjunctive technologies improve outcomes, and aren’t just "nice to have." Surgeons have traditionally regarded sealants and adhesives as convenience factors, having rarely gotten a chance, down the road, to get a second look at the surgical site to see how such products improved how the wound healed. Finally, hospital administrators and payors have needed to see that tissue sealants and adhesives lead to overall economic benefits and improved clinical outcomes, and this has been very difficult for companies to demonstrate. In the length of time it’s taken companies to demonstrate these benefits, many surgical markets have been eroded by the adoption of minimally invasive procedures, decreasing the overall opportunity.

It appears that the climate is becoming more favorable, however, especially in Europe, according to European Markets for New and...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Medtech Insight for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Europe

Aneira Health Launches New Precision Medicine Platform Exclusively For Women

 

Cecilia Lindgren, Aneira Health’s co-founder and chief science officer, said that the company has “redesigned the diagnostic model.” The subscription-based platform offers clinical-grade and AI diagnostics alongside clinical consultation.

AI In Health Delivery: Patients Most Confident When HCPs Are In Charge

 
• By 

Annual survey of patients and professionals shows how attitudes to health system transformation are evolving and what stakeholders are demanding as acceptance of AI tools accelerates.

Johnson & Johnson MedTech: How To Scale Digital Solutions

 

J&J's EMEA head of digital solutions, Julia Fishman, talks about the major hurdles in scaling digital innovation, tips for clinical adoption and what’s up next on J&J’s innovation road map. Robot-assisted surgery pioneer Ivo Broeders gives his perspective on the difficulties in clinical adoption.

EU Finalizes Framework For Joint Clinical Assessments Of High-Risk Devices

 

Second submission window for joint scientific consultations on a procedure to help prepare for joint clinical assessments will open from 2 to 30 June 2025.

More from Geography

FDA Outlines Responsibilities For Owners Of Transferred 510(k)s

 
• By 

The US FDA's new draft guidance details the responsibilities of new owners of 510(k) clearances, including making timely updates device listings in FURLS and GUDID to maintain accurate information for safety alerts and recalls. Comments on the draft are accepted until 4 August.

US House Budget Sets FDA FY26 Funding At $3.2B

 

A US House bill would give the FDA $33.1m more in budget authority than requested by the Trump Administration for fiscal year 2026. The measure was sent to the full House Appropriations committee on a party-line vote.

Panel: FDA’s Home Healthcare Initiative Holds Promise, But Challenges Remain

 
• By 

During a recent FDLI panel, experts discussed the FDA's Home Healthcare initiative, highlighting its potential benefits and challenges. Key issues include usability testing, reimbursement, labeling for home use, and the need for innovation while ensuring patient safety.