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Syneron Medical, an innovator in the development, marketing and sales of ELOS
combined-energy medical aesthetic devices, has announced it intends to file
a registration statement with the SEC for a public offering of up to 8,050,000
of its ordinary shares.
Biosite, a research-based provider of novel, rapid medical diagnostics, has
exercised a semi-exclusive license for research and diagnostic purposes to a
proprietary target, and has received an exclusive option to obtain licenses
for 50 other diagnostic targets, under its collaboration and license agreement
with Incyte.
Abbott has entered into a licensing agreement with The Cleveland Clinic for
the development of an automated in vitro diagnostic test to detect myeloperoxidase
(MPO), an enzyme found in white blood cells.
HemoGenix has made available its proprietary OxyFLOW Research Kit. HemoGenix,
in collaboration with Biotrin International, developed a flow cytometric assay
for detecting and quantifying oxidative DNA damage to lympho-hematopoietic cells.
A U.S.-based medical devices company, LMA International,
is preparing for a Singapore listing in a move that will test the local appetite
for companies operating in the high-risk, high-growth biomedical industry.
Vivosonic, a Toronto-based medical device developer, has announced FDA approval
for Integrity, a wireless objective hearing-assessment system, the company said.
St. Jude has announced the European market launch of the QuickSite 1056T bipolar
left-heart pacing lead, the world's first cardiac resynchronization therapy
lead to combine bipolar pacing capability with a composite body for superior
handling and a unique S-shaped distal tip for outstanding stability.
The FDA has reissued a nationwide alert against the use of all lots of preloaded
syringes containing either heparin or sodium chloride intravenous catheter flushes
manufactured by IV Flush and distributed by Pinnacle Medical Supply of Rowlett,
Texas.