Biomonde is one of 5120 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.
Biomonde — FDA 510(k) Products and Clearance History
2 devices
Cleared
Nov 05, 2014
LARVAL DEBRIDEMENT THERAPY PRODUCTS - LARVAE 100/200/300 AND BIOBAG...
General & Plastic Surgery
103d
Cleared
Aug 28, 2013
LARVAL DEBRIDEMENT THERAPY PRODUCTS - BIOBAG 50/100/200/300/400
General & Plastic Surgery
120d