Biomet, a manufacturer of orthopedic and biotechnology products, has announced the first US implantation of its Comprehensive nano stemless shoulder as part of an US Food and Drug Administration investigational device exemption (IDE) ...
Tags: Biomet, Nano Stemless Shoulder
St. Jude Medical, a global medical device company, has completed the acquisition of Nanostim, a developer of miniaturized, leadless pacemakers. St. Jude Medical and Nanostim have entered into a series of agreements in May 2011, pursuant ...
Tags: St.Jude Medical, medical device
Neuros Medical, a US-based neurostimulation company, has obtained an investigational device exemption (IDE) clearance from the US Food and Drug Administration (FDA) to initiate a randomized, controlled pivotal clinical trial to evaluate the ...
Tags: Neuros Medical, Altius System
US-based Crosstrees Medical has obtained 510(k) approval from the US Food and Drug Administration (FDA) for the Crosstrees PVA pod system for percutaneous vertebral augmentation (PVA). The FDA approval for the CE marked Crosstrees PVA pod ...
US-based medical device company Neuros Medical has obtained an investigational device exemption (IDE) approval from the US Food and Drug Administration (FDA) for its Altius, an implantable generator that delivers high frequency Electrical ...
Tags: Implantable Generator, Medicine
US-based medical device company TherOx has successfully completed the patient enrollment in its multicenter investigational device exemption (IDE) pilot study to evaluate the second generation system that delivers supersaturated oxygen ...
Israel-based medical device company Brainsway has received an investigational device exemption (IDE) from the US Food and Drug Administration (FDA) to evaluate the efficacy of its Deep TMS device in multi-center smoking cessation study. ...
Tags: Smoking Cessation Study, Health, Medicine
Mulpha Australia, the owner of Hayman Island, has selected the IDE PROGREEN? reverse osmosis system from IDE Technologies to provide high-quality desalinated water to the island resort. Hayman is a luxury, five star island resort located ...
US-based Moirai Orthopaedics has obtained CE Mark approval for its new Pyrocarbon Implant Replacement (PIR) system, designed to treat patients with focal chondral and osteochondral defects of the medial femoral condyle of the knee. The ...
PFM Medical, a developer and manufacturer of minimally invasive medical devices for cardio vascular technology, vascular access, surgery, and oncology, has received the US Food and Drug Administration (FDA) premarket approval for its ...
Tags: PFM Medical, Medicine
Medtronic has submitted its first pre-market approval (PMA) module to the U.S. Food and Drug Administration (FDA) for the IN.PACT Admiral drug-eluting balloon designed to treat atherosclerotic lesions in the superficial femoral artery ...
Tags: Medtronic, Admiral Drug-Eluting
Both sets of technologies recognize the growing use of the browser for richer interactions between users and services, over and above the viewing of static Web pages. “We still use the browser language, although most of what people ...
Hoping to generate more apps for its mobile platform, Microsoft has launched an online tool that could allow even non-developers to create new programs for Windows Phone 8. The tool, called Windows Phone App Studio, is free to use and in ...
Tags: Microsoft, Windows Phone
LDR has received a letter of approval from the US Food and Drug Administration (FDA) for commercial sale and distribution of its Mobi-C Cervical Disc (Mobi-C), for one-level indications in the US. The Mobi-C is designed for cervical disc ...
Tags: Mobi-C Cervical Disc
Mulpha Australia will use IDE Technologies' IDE PROGREEN modular reverse osmosis (RO) desalination solution to provide desalinated water for its Hayman island resort on the Great Barrier Reef. The IDE PROGREEN 'desalination plant-in-a-box' ...