Collafirm, LLC is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Collafirm, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Collafirm, LLC has 2 FDA 510(k) cleared medical devices. Based in Monmouth Jct, US.
Historical record: 2 cleared submissions from 2013 to 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Collafirm, LLC Filter by specialty or product code using the sidebar.
Collafirm, LLC — FDA 510(k) Products and Clearance History
2 devices
Cleared
Dec 22, 2014
BOVINE PERICARDIUM PATCH
General & Plastic Surgery
180d
Cleared
Apr 21, 2013
FIBRILLAR COLLAGEN WOUND DRESSING
General & Plastic Surgery
450d