Vessel sealing
LigaSure™ technology
25 years, 35 million procedures†,1–3 .
Performance you can trust for today and beyond.
The LigaSure™ XP Maryland jaw sealer-divider adds another chapter to our rich history of LigaSure™ 5mm laparoscopic devices.
Older LigaSure devices may not be liacensed in accordance with Canadian Law.
The LigaSure™ 8 device debuts as part of the world’s first energy-based ligation system.
The LigaSure™ V (dolphin tip) device is our first 5mm laparoscopic device with an integrated blade.
Launch of the LigaSure™ blunt tip device.
The LigaSure™ Advance device is added to the portfolio.
The next generation of LigaSure™ blunt tip provides the confidence of a latching handle.
The first-generation LigaSure™ Maryland jaw device is released, featuring a curved jaw and one-step activation.
LigaSure™ L-hook devices with retractable monopolar hook are added to the LigaSure™ family.
A new generation of LigaSure™ blunt tip and Maryland jaw devices incorporate nano-coating technology.
The LigaSure™ 8 device debuts as part of the world’s first energy-based ligation system.
The LigaSure™ V (dolphin tip) device is our first 5mm laparoscopic device with an integrated blade.
Launch of the LigaSure™ blunt tip device.
The LigaSure™ Advance device is added to the portfolio.
The next generation of LigaSure™ blunt tip provides the confidence of a latching handle.
The first-generation LigaSure™ Maryland jaw device is released, featuring a curved jaw and one-step activation.
LigaSure™ L-hook devices with retractable monopolar hook are added to the LigaSure™ family.
A new generation of LigaSure™ blunt tip and Maryland jaw devices incorporate nano-coating technology.
Introduction of the LigaSure™ XP Maryland jaw sealer-divider takes vessel sealing technology to the next level, evolving to integrate all the best features of the devices preceding it.
Discover the LigaSure™ technology suite of products and learn how they can help meet your procedural needs. (01:20)
Medtronic does not reprocess LigaSure™ vessel sealing devices
Testing showed critical differences in reprocessed vs. original vessel-sealing devices. 96% reprocessed vessel sealers failed a mix of 4 different tests that check for organic material4‡. Read the full study and learn more about the benefits of original Medtronic LigaSure™ devices.
Stryker reprocessed vessel sealing devices have contamination under the seal plates.4§ Read the full study and learn more about the benefits of original Medtronic LigaSure™ devices.
Medtronic provided funding, and sourced and supplied the devices. Data interpretation and analysis was performed solely by the authors, and Medtronic provided editorial support in accordance with Good Publication Practice guidelines.
Our impact
We put people and planet first, guided by environmental, social, and governance priorities.
† Based on global internal test report data FY01-FY23. November 2023.
‡ Sterility assurance level of 10^-6 accepted by the FDA as laid out in the Association for the Advancement of Medical Instrumentation (AAMI) standards ST67 and TIR 12 for devices contacting normally sterile tissue.
§ Contamination was found following disassembly of the devices and jaws. The study found that 52% of reprocessed devices studied had visible contamination. The remaining 48% did not have contamination that was visible to the naked eye.
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