Biomonde is one of 23263 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biomonde - FDA 510(k) Cleared Devices
Recent clearances: LARVAL DEBRIDEMENT THERAPY PRODUCTS - LARVAE 100/200/300 AND BIOBAG 50/100/200/300/400, LARVAL DEBRIDEMENT THERAPY PRODUCTS - BIOBAG 50/100/200/300/400
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