to Deliver the Industry’s Best File-sharing Capabilities with Integrated SMB Protocol for OEMs Through Better Interoperability Between Windows and Non-Windows Machines
NVIDIA and Mellanox just announced that NVIDIA has agreed to a cash purchase of all issued and outstanding common stock at a price of $125/share.
This version includes a number of new features: internal packet capture including IPv6, DNS and Netbios traffic, an enhanced mount command, and an enhanced directory lookup with pattern matching.
The Israel Innovation Authority and Startup Nation Central recently released the Human Capital Survey Report 2018. You can download it here.
Watch CEO & Founder of EyeCue, Ronen Horovitz discuss their "Do It Yourself" 3D scanning with Yoni Kempinski of Arutz Sheva.
Mr. Ahrens joins Mellanox from GlobalLogic, where he served as CFO . Prior to that he served as CFO of Applied Micro Circuits.
The treatment is given with a device small butterfly-shaped stent, which lifts the prostate's lobes and supports them so that they do not squeeze the urethra and cause it to narrow. The device, developed by Butterfly Medical, does not meet the urinary fluid and therefore does not expose patients to the risk of infection and stones. The patients who received the treatment reported that they did not feel the implant and did not experience any pain.
InMode Ltd. announced on Nov. 26 that the FDA has advised the company of satisfactory address of all items that appeared in the ‘It Has Come to Our Attention’ letter.
On July 24th 2018, InMode, along with many other aesthetic laser companies, received an “It Has Come to Our Attention” letter. InMode has been communicating with the FDA to specify all FDA clearances and listings of the Votiva platform, and on November 9th 2018, InMode received notice stating that: “FDA determined that it appears your firm has addressed all items found in the ‘It Has Come to Our Attention’ letter.”
InMode is committed to work in full collaboration with the FDA and, as discussed with FDA, will continue to review its marketing and promotional material to assure full compliance with the FDA clearances and listings for the Votiva platform, and any other platforms marketed by InMode.
“We are pleased that the FDA has accepted our response in full. We will continue to market our Votiva platforms in accordance with FDA guidelines and regulations, and in accordance with the Votiva platform clearances and listings. InMode will continue to develop products for the rapidly-growing women’s health and wellness market,” said Shakil Lakhani, President of InMode, North America.
InMode is a leading global provider of innovative, energy-based, minimally and non-invasive aesthetic solutions. InMode has developed and commercialized products utilizing medically-accepted radiofrequency energy technology, which can penetrate deep into the subdermal fat, allowing adipose tissue remodelling. InMode’s technologies are used by physicians to remodel subdermal adipose, or fatty tissue, in a variety of procedures including liposuction with simultaneous skin tightening, face and body contouring, ablative skin treatments and women’s health and wellness procedures. Learn more about InMode technologies by visiting www.inmodemd.com.
Provider of Japan’s Largest Messaging App Deploys Mellanox Open Ethernet Switches Running Cumulus Linux in 1000+ Switches, Tens of Thousands of Compute Nodes Data Center
AdaSky intends to use the investment to continue developing its thermal FIR sensor, which is incorporated in autonomous vehicles and ADAS systems.