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KLOX Technologies annonce qu'elle a obtenu l'approbation européenne du marquage CE sur son produit novateur et non invasif pour l'acné simple
Date:11/19/2013

LAVAL, Québec, November 19, 2013 /PRNewswire/ --

LumiCleanse[TM]est un traitement cliniquement prouvé maintenant disponible pour tous les degrés de sévérité de l'acné simple mis au point par KLOX au Canada et destiné au marché mondial de l'acné

KLOX Technologies inc. (« KLOX » ou la « Société ») est heureuse d'annoncer qu'elle a obtenu l'approbation de marquage CE en Europe pour son gel convertisseur-photo topique à titre d'appareil médical de catégorie IIa pour le traitement de l'acné simple, y compris pour tout type de gravité. Le gel fait partie du système LumiCleanse[TM] de KLOX, une nouvelle classe de traitement novateur et non invasif de l'acné simple disposant d'un profil d'innocuité et d'efficacité supérieur, cliniquement prouvé. Le système LumiCleanse[TM] a déjà été approuvé pour le traitement de toutes les gravités d'acné simple au Canada en septembre de cette année.

« Nous sommes ravis de franchir cette nouvelle étape dans notre stratégie réglementaire et commerciale ainsi que dans nos efforts visant à accroître la portée du traitement innovant de KLOX dans le marché mondial de l'acné de 3 milliards $. L'Europe offre un important bassin de patients potentiels qui ne trouvent pas réponse à leurs besoins en matière de traitement efficace de l'acné légère à sévère », a déclaré D[re] Lise Hébert, présidente et chef de la direction de KLOX.

La preuve clinique au
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SOURCE Klox Technologies Inc.
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