A landmark three-dimensional (3-D) digital reconstruction of a complete human brain, called the BigBrain, now for the first time shows the brain anatomy in microscopic detail—at a spatial resolution of 20 microns, smaller than the size of one fine strand of hair—exceeding that of existing reference brains presently in the public domain.
Lumosity, the leading brain training company, today announced a new web-based, big data methodology for conducting human cognitive performance research. Lumosity's research platform, the Human Cognition Project, contains the world's largest and continuously growing dataset of human cognitive performance, which currently includes more than 40 million people who have been tracked for up to 6 years.
RegeneCure announced today the start of a clinical study using the company's proprietary AMCA Guided Bone Regeneration (GBR) Dental Membrane as a bone stimulating aid for patients requiring dental implants. A common problem encountered when patients have a tooth replaced with a dental implant is the lack of sufficient bone volume to house the implant.
Royal Philips (NYSE: PHG, AEX: PHIA) today announced new capabilities for its Iterative Model Reconstruction (IMR) technology, a knowledge-based iterative reconstruction technique, that will simultaneously bring enhanced benefits to clinicians and patients.
CryoLife, Inc. (NYSE: CRY), a leading tissue processing and medical device Company focused on cardiac and vascular surgery, announced today that it has received conditional approval of its Investigational Device Exemption (IDE) for PerClot from the United States Food and Drug Administration (FDA).
Covidien (NYSE:COV), a leading global provider of healthcare products, today announced that the final results of the PUFs (Pipeline for Uncoilable or Failed Aneurysms) clinical study of its Pipeline™ embolization device have been published in the June issue of Radiology. Radiology is the official peer-reviewed medical journal of the Radiological Society of North America.
The firm received complaints of "cuff leak" or "cuff deflation" occurring when the inflation valve cap is inappropriately removed (pulled off, instead of snapped-off sideways). This requires the physician to re-inflate or replace the deflated tube to ensure the continued breathing support of the patient. Use of this recalled product can result in serious adverse health consequences, including death.
Specialty Coating Systems has announced a significant breakthrough in Parylene coating technologies: SCS microRESIST Antimicrobial Parylene Technology. SCS microRESIST combines the benefits of biocompatible Parylene with antimicrobial properties to effectively eliminate harmful microorganisms on coated medical devices.
Foster Corporation has introduced ProPell thermoplastic polyurethane and polyether block amide compounds for improved manufacturing and handling of medical catheters. These new compounds dramatically reduce tackiness and friction in soft, flexible polymers while maintaining other physical properties of the unmodified polymers.
Connor-Winfield’s newest OXCO, the OX200-SC is our most quiet, accurate and stable 10.0 MHz OCXO. The OX200-SC is designed for use in applications such as IP Backhaul using IEEE1588 PTP Master Clock that requires very high frequency stability, very tight initial calibration and very low aging.
Given the number of device applications that involve the transfer of a gas or liquid, it is no wonder pump technology is such a significant part of many healthcare-related products. In addition, pumps are not exempt from the trends of miniaturization and cost reduction. As such, this article takes a look at how today’s medical device demands are being answered by advanced pump technology.
Colson Caster has announced its newest line of heavy duty wheels for mass distribution: the Commander HD. The innovative wheel is designed for superior performance in some of the most abusive applications and environments where high-load requirements and impact resistance are a must.
The Food and Drug Administration said last Friday it approved a next-generation silicone breast implant from Johnson & Johnson unit Mentor. The company's MemoryShape breast implant uses a cross-linking gel design that the FDA says is firmer than previous implants.
Synergy Biomedical, LLC has announced that it has recently received FDA clearance and will be launching its first bone graft product, BioSphere™ Putty. Utilizing a specialized form of 45S5 bioactive glass with a unique sphere shape and a narrow size range, BioSphere™ Putty provides an optimized bone graft material that outperforms other bioactive products.
Around 15 years ago, I was fortunate enough to study for a Ph.D. with an Entrepreneurial Professor. Five years later, after working on a few healthcare-related projects, we were then fortunate enough to snag an ambitious MBA graduate with an executive retail background, looking for a new challenge, and gained support of doctors.