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Post Info TOPIC: Intacs Gains FDA Designation as Corneal Implants
Anonymous

Date: Mon Jan 9 4:25 AM, 2006
Intacs Gains FDA Designation as Corneal Implants
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Press Release from Addition Technology regarding Intacs:



Intacs Gains FDA Designation as "Corneal Implants"



Des Plaines, IL (Jan. 4, 2006) - The U.S. Food and Drug Administration
(FDA)
has granted Addition Technology, Inc., the use of the term "corneal
implants" to describe Intacs, heretofore referred to as "prescription
inserts."



"We are pleased with the FDA's recognition of Intacs as a therapeutic
device. Surgeons around the world have been utilizing Intacs as a
mainstay
problem-solver for keratoconus and ectasia in corneal and refractive
surgery
and this designation assists in clarifying the appropriate positioning.
2005
saw us report our twelfth consecutive quarter of double-digit sales
growth,"
said William Flynn, chief executive officer of Addition Technology.



"The positioning of Intacs as a therapeutic device will result in new
levels
of sales and growth in 2006," predicted Flynn. "As Addition Technology
has
achieved critical mass, we look forward to further expanding the
benefit of
Intacs for surgeons and their patients around the globe. Intacs is also
beginning to be recognized by refractive surgeons as a safe alternative
for
the two to three percent of mildly nearsighted patients desiring
refractive
surgery for whom tissue ablation or intraocular surgery are not ideal."



Addition Technology, Inc., a privately held company, manufactures
Intacs,
the only additive corneal implant approved by the U.S. Food and Drug
Administration for both keratoconus and myopia. Intacs also are
approved for
use in Europe, Asia, Mexico and parts of Latin America. For more
information, visit http://www.IntacsForKeratoconus.com


-- Edited by QuintriX at 20:33, 2006-03-24

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