Biomonde is one of 5629 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biomonde - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Biomonde has 2 FDA 510(k) cleared medical devices. Based in Marlborough, US.
Historical record: 2 cleared submissions from 2013 to 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Biomonde Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biomonde
2 devices