The US Food and Drug Administration(FDA)has approved Ethicon Biosurgery's new fibrin sealant patch to aid surgeons in stopping problematic bleeding during surgery. The fibrin sealant patch,EVARREST,comprises a coating of biologics(human ...
US-based manufacturer of bar code label printing software Tharo Systems has announced the launch of its new Easylabel 5 GS1 Barcode Wizard that features two GS1 wizards. The wizards include GS1 Datamatrix and GS1 Databar, ...
Tags: label printing, labels, packaging, printing
UK-based Newman Labelling Systems is set to introduce its new NVS2 labeling system, which is fully automatic and has been designed specifically for use with glass or plastic syringes and other similar cylindrical containers. The ...
Tags: labeling system, labels, packaging, printing
BG Medicine has registered a 510(k) premarket notification with the US Food and Drug Administration (FDA) for approval of its Architect Galectin-3 assay. The Architect Galectin-3 assay, which is designed for use with Abbott's automated ...
Tags: BG Medicine, premarket notification, FDA, Architect Galectin-3 assay
UK-based Almac, a provider of contract services to pharmaceutical and biotech industries, has announced that it has expanded its MHRA/FDA approved UK commercial packaging facility, following its acquisition of a Noack N 623 blister ...
Tags: blister packaging, Almac, packaging facility
HTG Molecular Diagnostics has partnered John Wayne Cancer Institute (JWCI) to sell its HTG melanoma signature assays. The signature assays are intended to be useful for diagnostic and prognostic applications along the melanoma continuum. ...
Tags: HTG Molecular, JWCI, melanoma signature, signature assays
GI Dynamics has obtained conditional approval from the US Food and Drug Administration (FDA) to initiate a pivotal clinical trial of its non-surgical EndoBarrier device. Flexible, tube-shaped EndoBarrier liner, which forms a physical ...
Tags: GI Dynamics, conditional approval, FDA, pivotal clinical trial
The US Food and Drug Administration (FDA) has granted 510(k) approval to Medtronic's Aquamantys3 BSC 9.1S bipolar sealer with cutting, designed for use in orthopaedic surgery. By utilizing Transcollation technology, the BSC 9.1S Bipolar ...
Tags: FDA, 510(k)approval, orthopaedic surgery, transcollation technology
The European Union has granted CE mark approval to InSightec's transcranial focused ultrasound system for the treatment of essential tremor, tremor dominant Parkinson's disease and neuropathic pain. The non-invasive ExAblate Neuro ...
Tags: transcranial focused ultrasound system, Parkinson's disease
The US Food and Drug Administration (FDA) has granted 510(k) clearance to Biosign Technologies' non-invasive blood pressure measurement system, Pulsewave monitor. The UFIT EN-10 monitor is worn on the wrist having 13.5 cm to 23 cm (5.3 ...
Tags: FDA, blood pressure measurement system, pulsewave monitor, systolic
Precision Spine, the parent company of Spinal USA, has announced FDA 510(k) clearance of the Slimplicity solo anterior cervical plate system. The Spinal USA's Slimplicity new anterior cervical plate system, which consists of one and two ...
Tags: Spinal USA, FDA 510(k)clearance, solo anterior cervical plate system
Vestcom, a provider of marketing services for the retail industry, has expanded its health and wellness in-store marketing program with the integration of US Department of Agriculture (USDA) data for fresh meat, seafood and produce. ...
Tags: marketing services, retail industry, health and wellness
S&P of California is recalling 1800 jars of its Su-nun Crush Roasted Thai Red Pepper due to possible Salmonella contamination, according to the US Food and Drug Administration (FDA). The recall was initiated after a routine sampling by ...
Tags: salmonella contamination, routine sampling, weakened immune systems
Teva Women's Health, a US-based subsidiary of Teva Pharmaceutical Industries, has announced FDA acceptance of its Quartette new drug application (NDA). The company is seeking approval to manufacture and market Quartette ...
Tags: ethinyl estradiol tablets, market Quartette, contraceptive products
The Food and Drug Administration (FDA) has accepted Dynavax Technologies' heplisav biologics license application (BLA) for immunization against infection caused by all known subtypes of hepatitis B virus in adults 18 through 70 years of ...