Progenika Biopharma S.A., A Grifols Company is one of 56 FDA 510(k) medical device manufacturers from Spain in the dataset, ranked by real submission volume.
Progenika Biopharma S.A., A Grifols Company - FDA 510(k) Cleared Devi...
Recent clearances: AlphaID™ At Home Genetic Health Risk Service, A1AT Genotyping Test, A1AT Genotyping Test
4
Total
4
Cleared
0
Denied
Progenika Biopharma S.A., A Grifols Company has 4 FDA 510(k) cleared medical devices. Based in Derio, ES.
Last cleared in 2022. Active since 2017. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Progenika Biopharma S.A., A Grifols Company Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Progenika Biopharma S.A., A Grifols Company
4 devices