Uniderm Farmaceutici Srl is one of 222 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Uniderm Farmaceutici Srl - FDA 510(k) Cleared Devices
Recent clearances: Lubrigyn cream, LUBRIGYN CREAM
2
Total
2
Cleared
0
Denied
Uniderm Farmaceutici Srl has 2 FDA 510(k) cleared medical devices. Based in Imola, Bo, IT.
Historical record: 2 cleared submissions from 2014 to 2015. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Uniderm Farmaceutici Srl Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Isemed S.R.L. as regulatory consultant.
FDA 510(k) Regulatory Record - Uniderm Farmaceutici Srl
2 devices