Hogan Lovells counsels Bioretec in first ever De Novo grant for bioresorbable metal trauma screw. Bioretec Ltd., a pioneer in bioresorbable orthopedic implants, in securing Food...
Bioretec Ltd’s Obtaining FDA Premarket Authorization for RemeOs Trauma Screw
P-Cure’s FDA Market Authorization of New Proton Therapy Device for Cancer Treatment
Hogan Lovells advised P-Cure in the authorization process. P-Cure, an Israeli med-tech company, in U.S. Food and Drug Administration (FDA) market clearance for a proton therapy...
Lucira Health’s OTC COVID-19 and Flu Test FDA Authorisation
Hogan Lovells counseled Lucira Health, Inc. Lucira Health, Inc. (Lucira), a medical technology company focused on the development of innovative infectious disease tests, secured U.S. Food...
Apollo Endosurgery’s FDA Market Authorization for Endoscopic Sleeve Gastroplasty and Endoscopic Bariatric Revision Devices
Hogan Lovells advised Apollo Endosurgery, Inc. on the deal. Apollo Endosurgery, Inc., a global leader in minimally invasive medical devices for gastrointestinal and bariatric procedures, in...
NONAGON’s FDA 510(k) Clearance For Smartphone Compatible Telehealth Device
Hogan Lovells advised NONAGON on the deal. NONAGON (previously named MyHomeDoc) through the U.S. Food and Drug Administration 510(k) clearance process for its N9 multisensory device...