Teleflex Receives FDA Clearance for Reusable Obturators

Teleflex has announced it has received FDA clearance for a line of reusable obturators, according to a news release.

 

The Weck reusable obturators are designed to complement the company's Weck Vista line of bladeless laparoscopic access ports, according to the company. The obturators are compatible with Weck Vista single-use cannula options.

 

"We are conscious of the patients' needs and the challenges faced by surgeons in the operating room," said Jay White, vice president and general manager, surgical division, for Teleflex, in the release. "By expanding our line of access to include these new reusable obturators, Teleflex continues to affirm its commitment to addressing these needs and providing effective solutions that help enhance patient safety."

 

Teleflex is headquartered in Limerick, Pa.

 

Related Articles on FDA Clearances:

MAQUET Cardiovascular Receives FDA Clearance for Intra-Aortic Balloon Catheter

Providence Medical Technology Receives FDA Clearance for Bone Screws

Osseon Receives FDA Clearance for Steerable Inflatable Bone Tamp

Copyright © 2024 Becker's Healthcare. All Rights Reserved. Privacy Policy. Cookie Policy. Linking and Reprinting Policy.

 

Featured Webinars

Featured Whitepapers