Unibell S.R.L is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Unibell S.R.L - FDA 510(k) Cleared Devices
Recent clearances: Human Tecar HCR 1002
1
Total
1
Cleared
0
Denied
Unibell S.R.L has 1 FDA 510(k) cleared medical devices. Based in Calco, IT.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Unibell S.R.L Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by THEMA S.r.l. as regulatory consultant.
FDA 510(k) Regulatory Record - Unibell S.R.L
1 devices