Collamatrix Co., Inc. is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Collamatrix Co., Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Collamatrix Co., Inc. has 4 FDA 510(k) cleared medical devices. Based in Taipei, TW.
Historical record: 4 cleared submissions from 2006 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Collamatrix Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Collamatrix Co., Inc.
4 devices
Cleared
Jun 25, 2009
COLLAWOUND WOUND DRESSING
General & Plastic Surgery
86d
Cleared
Feb 08, 2008
COLLAWOUND HYDROGEL
General & Plastic Surgery
246d
Cleared
Mar 02, 2007
MODIFICATION TO COLLAWOUND DRESSING
General & Plastic Surgery
32d
Cleared
Jul 05, 2006
COLLAWOUND DRESSING
General & Plastic Surgery
36d