"Receiving FDA 510(k) clearance for this device was an important milestone for Paragon. Now receiving the CE mark approval will allow additional commercialization throughout the European Union. In keeping with Paragon's ultimate goal to protect and preserve eyesight, the Comfortear(R) Lacrisolve(TM) Absorbable Punctum Plug is a great addition to our portfolio of ophthalmic products," said Lauren M-C Bluett, Director of Quality Assurance.
About Comfortear(R) Lacrisolve(TM) Absorbable Punctum Plug:
Comprised of the synthetic absorbable polymer, polydioxanone, the Comfortear(R) Lacrisolve(TM) Absorbable Punctum Plugs are medium-term implants designed to be inserted into the canaliculus in order to block tear drainage through the lacrimal drainage system. The Comfortear(R) Lacrisolve(TM) Absorbable Punctum Plugs are available in two diameters: 0.4mm and 0.5mm. The implants are supplied sterile with two implants per package.
Absorption time for the Comfortear(R) Lacrisolve(TM) Absorbable Punctum Plugs is approximately 6 months (=<6). For full prescribing information, visit http://paragonbioteck.com/products/ .
About Paragon BioTeck, Inc.:
Paragon BioTeck, Inc. is a privately held ophthalmic-focused biopharmaceutical and medical device company pursuing the development and commercialization of products addressing unmet medical needs in the fight to protect and preserve eyesight. For more information on the company and its work, visit http://www.paragonbioteck.com/ .
For more information please call 888-424-1192 or email to info@paragonbioteck.com.
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*Caption: Comfortear(R) Lacrisolve(TM) Absorbable Punctum Plugs.
NEWS SOURCE: Paragon BioTeck, Inc. :: This press release was issued on behalf of the news source (who is solely responsible for its accuracy) by Send2Press® Newswire, a service of Neotrope®.