Biotekne Srl is one of 221 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Biotekne Srl - FDA 510(k) Cleared Devices
Recent clearances: meso-relle (AAL34, AAL36, AM30G)
1
Total
1
Cleared
0
Denied
Biotekne Srl has 1 FDA 510(k) cleared medical devices. Based in Casalecchio Di Reno, IT.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Biotekne Srl Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Studio DI Ingegneria Enrico Bisson as regulatory consultant.
FDA 510(k) Regulatory Record - Biotekne Srl
1 devices