Medtech Insight is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction

Greatbatch acquisition strengthens design capabilities

This article was originally published in The Gray Sheet

Executive Summary

Implantable cardioverter defibrillator component maker Greatbatch will pay $11.4 million in cash to acquire Biomec in an effort to expand its device design and engineering services, the firm announces March 19. Cleveland, Ohio-based Biomec is developing a polymer coating that mimics the surface of endothelial cells of blood vessels. The coating, for use on medical devices ranging from catheters to blood pump circuits, is intended to reduce the risk of clotting, inflammation and infection. Greatbatch also assumes Biomec's minority ownership in IntElect Medical, which is developing a neurostimulation device for stroke and traumatic brain injury. The deal is expected to close shortly after a Biomec shareholder vote on April 3, according to a Greatbatch spokesperson...

You may also be interested in...



Greatbatch To Boost Cardiac And Neurostim Presence With Enpath Purchase

Greatbatch hopes to expand its reach in the cardiac rhythm management and neurostimulation markets with a $102 million acquisition of Enpath announced April 30

Xbrane Assembles The Troops As FDA Says No To Lucentis Biosimilar

Xbrane Biopharma was riding the crest of a wave with the EU launch of its biosimilar to Lucentis, following years of toil and investment. However, plans to roll out the product in the US will have to be pushed back – likely – into the middle of 2025, following a US FDA complete response letter.

UK MHRA Updates Assistive Tech And Borderline Regulations

Device classification themes were uppermost in April for the UK regulator, which issued key guidance in two areas prone to complexities. It also contributed to the MedTech Directorate’s one-year progress report.

Latest Headlines
See All
UsernamePublicRestriction

Register

MT024622

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel