Megadyne Medical Products
In 1985, our electrosurgical device company, Megadyne, was founded with the launch of our E-Z Clean® line of non-stick, eschar-resistant, PTFE-coated electrodes. Today, we are recognized as the authority on non-stick electrosurgical electrodes.
From the start, Megadyne has strived to provide high-quality products that are also cost effective for the benefit of surgeons, nurses, and hospitals. Located in Draper, Utah, Megadyne Medical has been in operation for over thirty years. Our research and development teams have remained consistently innovative when it comes to providing revolutionary electrosurgical devices for healthcare professionals at a pace that matches the constant changes in their field of work.
Thousands of operating rooms all over the world use Megadyne products, and they have been proven time and again for their effectiveness. This has been Megadyne’s driving force behind their emergent success in the medical products industry. While Megadyne started as an electrosurgery tool provider, we now stand strong as an electrosurgical device company that provides healthcare professionals with start-to-finish solutions including electrosurgical equipment and accessories.
Megadyne offers numerous electrosurgical products including: the E-Z Clean® line of non-stick electrosurgical tips, the E-Z Pen™ Electrosurgical Pencil, the Mega Power® Electrosurgical Generator, Resposable Laparoscopic Electrodes with MegaTip® and Indicator Shaft® technology, and the revolutionary reusable Mega Soft® Patient Return Electrode System. In addition to these exceptional electrosurgical devices, we also provide open procedure electrodes, electrosurgical pencils, bipolar forceps, laparoscopic electrodes, and a myriad of other electrosurgical accessories.
Megadyne also offers grant funds to help nurses and surgeons continue their education through independent studies and courses in order to better maintain our high training standards. To help ensure these standards of training, Megadyne upholds a certified Quality System that closely follows the requirements of:
US FDA 21 CFR Part 820,
Canada Medical Device Requirements,
European Medical Device Directive 93/42/EEC, and
Japan MHLW Ordinance No. 169