Klox Technologies Inc. Files a De Novo Classification Request with the U.S. Food and Drug Administration
LAVAL, Quebec, FEBRUARY 4, 2020 -- Klox Technologies, Inc. (‘Klox’), a regenerative medicine company focused on the development of its proprietary FLE biomodulation platform, today announced that it has filed a De Novo Classification Request with the US FDA for its LumiHeal System following receipt of device designation in late 2019.“This significant milestone represents Klox’s commitment to work with the US FDA and CDRH to deliver an innovative treatment modality for healthcare practitioners and patients alike within wound care” said Carlo Bellini, President of Klox. “We are currently in