Peptonic Medical submits 510k application for VagiVital® in the US
Stockholm, 25th February, 2020 – Peptonic Medical (publ) (“Peptonic” or “Company”) today announced that it has submitted a so called 510k application to the US Food and Drug Adminstration (FDA) to obtain approval to market and sell VagiVital® in the USA.- USA is the single largest market for vaginal atrophy products in the world, and we believe that VagiVital® is well positioned to successfully enter the self-care market segment thanks to its unique clinical proof of efficacy and safety, and for its effective symptom relief, says Johan Inborr, CEO of Peptonic Medical. The Company is