Uniderm Farmaceutici Srl is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Uniderm Farmaceutici Srl - FDA 510(k) Cleared Devices
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.
FDA 510(k) Regulatory Record - Uniderm Farmaceutici Srl
2 devices