Vibratory bowl feeders can be classified as an automation machine. These machines are used with the intention of mechanizing certain applications and reducing dependence on human labor. In view of an uncertain economic climate, many ...
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Natus Neurology has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) and Health Canada clearance for its new electrodiagnostic system, the UltraPro S100 EMG system. The UltraPro S100 is an EMG/nerve conduction ...
Wyss Institute for Biologically Inspired Engineering of Harvard University has secured a $5.6m contract from the U.S. Food and Drug Administration for its organs-on-chips technology to assess medical countermeasures for treating acute ...
ViiV Healthcare, HIV company established by GlaxoSmithKline and Pfizer, has announced the FDA approval of an integrase inhibitor, Tivicay (dolutegravir) 50mg tablets, for the treatment of HIV-1. Tivicay is indicated for use in combination ...
Tags: Viiv Healthcare, HIV-1
Danish drugmaker Lundbeck has announced the availability of ONFI (clobazam) in scored tablet and oral suspension formulations in the US pharmacies beginning this week. ONFI, an oral anti-epileptic drug (AED) of the benzodiazepine class, ...
American fresh-cut fruits and vegetables producer Taylor Farms has voluntarily suspended the production of salad mix and leafy greens at its facility in Mexico. The company notified the US Food and Drug Administration (FDA) that it has ...
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Medical technology provider Vidacare Corporation is planning to launch its single needle vascular access system called TALON (tactically advanced lifesaving intraosseous needle) for military personnel. TALON system provides combat life ...
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The US Food and Drug Administration (FDA) has cleared Given Imaging’s next-generation video capsule, called PillCam SB 3. The 11 mm x 26 mm video capsule is helpful in detecting small bowel abnormalities related to Crohn's disease, ...
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Quantel Medical has received the U.S. Food and Drug Administration (FDA) approval for its selective laser trabeculoplasty (SLT) glaucoma laser for clinical use, called Solutis. Solutis is a 532nm SLT laser designed for primary open angle ...
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The U.S. Food and Drug Administration published a new regulation defining the term "gluten-free" for voluntary food labeling. This will provide a uniform standard definition to help the up to 3 million Americans who have celiac disease, an ...
Tags: Packaging, Printing, food packaging
DeltaTRAK has launched a certified reusable data logger with glycol bottle, the FlashLink USB Data Logger with Glycol Bottle, compatible with CDC guidelines. Designed for monitoring temperatures of vaccines inside refrigerators or ...
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Pharmaceutical marketing, research and development company Breckenridge Pharmaceutical has signed a deal to acquire certain assets of Pernix Therapeutics' subsidiary, Cypress Pharmaceuticals, for $30m. The assets included in the agreement ...
The US Food and Drug Administration (FDA) has approved Alere's pre-market application (PMA) for the commercialization of Alere Determine HIV 1/2 Ag/Ab Combo in the country. The FDA approval allows the marketing of Alere Determine HIV 1/2 ...
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RTI Surgical, a manufacturer of orthopaedic and other biologic implants, has launched Tritium Sternal Cable Plating (SCP) system for closing median sternotomies following open heart procedures. The device incorporates the advantages of ...
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Verizon, a US- based broadband and telecommunications company, has received the US Food and Drug Administration (FDA) 510(k) clearance for a cloud-based, remote patient-monitoring medical device called Converged Health Management. ...
Tags: Verizon, Patient-Monitoring Device