The US Food and Drug Administration (FDA) is evaluating the safety of Intuitive Surgical's robotic surgical devices. Currently, the agency is studying a small group of surgeons who use the surgical device, which is used in over 2,000 ...
NEW YORK, June 6, 2013 /PRNewswire/ -- Sephora—the visionary beauty retailer—recently solidified its partnership with Silk'n to add the Silk'n Flash&Go Freedom hair removal device to select stores nationwide. Following the ...
The FDA has cleared Celgene's supplemental new drug application (sNDA) for Revlimid (lenalidomide) for the treatment of patients with relapsed or refractory mantle cell lymphoma (MCL). The approval follows positive data from MCL-001 phase ...
Creole, an establishment based in New Orleans, Louisiana, is recalling its 3.47oz. packs of Creole Bisque as the product contains milk, soy, and wheat which are not mentioned on the label. People who have allergies to milk, soy, and ...
Tags: Agriculture, Food
Cook Medical has received the 510(k) approval from the US Food and Drug Administration (FDA) for its Evolution Biliary Controlled-Release Uncovered Stent. Adding to the Cook's line of Evolution controlled-release stents for the ...
Tags: Cook Medical, Biliary Stent
Blue Belt, next generation surgical orthopedic instruments developer, has received 510(k) approval from the US Food and Drug Administration (FDA) to market its Stride Unicondylar Knee implant system. With the clearance, the Stride implant ...
Tags: Blue Belt, FDA Approval
Plastics these days have become requisite part of our daily life. Almost every industry and home makes use of it. According to the variation in molecular structure, plastics can be classified as thermoplastics or thermo sets. Keeping the ...
Tags: Plastics, Processing Machinery
Specialty pharmaceutical company Sun Pharmaceutical Industries has obtained final USFDA approval for the abbreviated new drug application of generic Depo-Testosterone Injection, Testosterone Cypionate Injection USP, 100mg/ml and 200mg/ml. ...
Medtronic has received both the US Food and Drug Administration (FDA) approval and the CE (Conformité Européenne) Mark clearance for its Pacific Plus percutaneous transluminal angioplasty (PTA), the new peripheral balloon ...
Tags: Angioplasty Balloon, Medicine
US-based establishment Finger Lakes Farmstead Cheese is recalling 12 wheels of Gouda cheese, as it may be contaminated with Listeria monocytogenes Type 1, according to the US Food and Drug Administration (FDA). The product associated with ...
Tags: cheese, Agriculture, Food
The US Food and Drug Administration (FDA) has approved GlaxoSmithKline's Tafinlar (dabrafenib) and Mekinist (trametinib) as single-agent therapies for unresectable or metastatic melanoma with BRAF V600E mutation. Tafinlar is not indicated ...
Polyacrylonitrile co-polymers supplier, Ineos Barex has signed a binding agreement to purchase the Polyacrylonitriles Business from Mitsui Chemicals for an undisclosed amount. The partnership deals with integrating complementary ...
Tags: Chemicals, Polyacrylonitrile
GE Healthcare has obtained 510(k) clearance from the US Food and Administration (FDA) for its Brivo Plus C-arm, which is made available now in the US. The approval is expected to transform healthcare in private practices and rural ...
Tags: Healthcare, Health&Medicine, FDA
The USFDA has accepted Teva Pharmaceutical Industries' supplemental new drug application (sNDA) for reviewing Copaxone (glatiramer acetate injection) 40mg/1mL. Indicated for patients with relapsing-remitting multiple sclerosis (RRMS), the ...
Tags: Drug Application, Medicine
Research-based biopharmaceutical company AbbVie has announced the availability of new, higher-dose of Creon (pancrelipase) delayed-release capsules in the US. Indicated for patients with exocrine pancreatic insufficiency (EPI), 36,000 ...