Biolase has obtained rights to market its new diode laser technology in the US and throughout the European Union (EU) and in those Asian and Latin American countries that recognize the CE mark. The EPIC 10 diode soft tissue laser utilizes ...
Tags: diode laser, diode soft tissue laser, laser
The US Food and Drug Administration (FDA) has cleared Crospon's EndoFLIP system for use in gastroenterology applications. The EndoFLIP system utilizes the new Barostat software to include pressure and dimension measurements taken in the ...
Tags: EndoFLIP system, Barostat software, FDA, gastroenterology applications
Genentech, a member of Roche Group, has obtained clearance for its Lucentis 0.3 mg (ranibizumab injection) from the US Food and Drug Administration (FDA). Lucentis 0.3 mg is a recombinant humanized monoclonal antibody fragment (lacking an ...
Tags: Genentech, Lucentis 0.3 mg, Medicine, Injection
US distribution deal for spectral blood sensor 03 Jul 2012 PSS World Medical to market Masimo's latest multi-wavelength spot-checker for hemoglobin,pulse rate and perfusion index. Pronto-7 oximeter Masimo Corporation,the US ...
Tags: spectral blood sensor, medical sensor, PSS World Medical
Dako, a Danish provider of cancer diagnostics solutions, has received approval from the US Food and Drug Administration to market HercepTest and HER2 FISH pharmDx Kit as companion diagnostics for pertuzumab (Perjeta) - a new Genentech ...
Tags: Dako, cancer diagnostics solutions, HercepTest, HER2 FISH
Ambit Biosciences and Teva Pharmaceutical Industries have announced the FDA clearance of CEP-32496, a novel BRAF (V600E) kinase inhibitor. The preclinical findings also demonstrate that CEP-32496 possesses potent and sustained anti-tumor ...
Tags: Ambit, Teva, FDA clearance