Biolitec Sia (Latvia) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biolitec Sia (Latvia) - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Biolitec Sia (Latvia) has 1 FDA 510(k) cleared medical devices. Based in Grandville, US.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Biolitec Sia (Latvia) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biolitec Sia (Latvia)
1 devices