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July 12, 2018 

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0:35 Recursion Receives FDA Clearance of Investigational New Drug Application to Initiate First Clinical Trial of REC-994 in Cerebral Cavernous Malformation

2:25 RedDress Receives FDA 510(k) Clearance for RD1 System. Innovative Device for Wound Management. 

3:27 Oculocare's Alleye® Receives FDA 510(k) clearance for monitoring Eyesight in AMD 

5:05 Bausch + Lomb Announces U.S. FDA Filing Acceptance For Loteprednol Etabonate Ophthalmic Gel, 0.38% 

6:01 OBI Pharma Granted FDA Orphan Drug Designation for OBI-3424 for the Treatment of Hepatocellular Carcinoma (HCC) 

8:11 FDA updates warnings for fluoroquinolone antibiotics on risks of mental health and low blood sugar adverse reaction 

10:20 Statement from FDA Commissioner Scott Gottlieb, M.D. on agency’s efforts to advance development of gene therapies

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