Marine Polymer Technologies, Inc. is one of 4740 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Marine Polymer Technologies, Inc. - FDA 510(k) Cleared Devices
8
Total
7
Cleared
0
Denied
Marine Polymer Technologies, Inc. has 7 FDA 510(k) cleared medical devices. Based in Danvers, US.
Historical record: 7 cleared submissions from 1997 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Marine Polymer Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Marine Polymer Technologies, Inc.
8 devices
Cleared
Dec 06, 2016
Talymed Suspension
General & Plastic Surgery
267d
Cleared
Jul 22, 2011
MP 719
General & Plastic Surgery
50d
Cleared
Oct 14, 2008
MRDH BANDAGE
General & Plastic Surgery
28d
Cleared
May 23, 2007
MP 719
General & Plastic Surgery
85d
Cleared
Mar 28, 2006
SYVEKEXCEL
Cardiovascular
123d
Cleared
Dec 20, 2000
RDH BANDAGE
General & Plastic Surgery
125d
Cleared
Dec 18, 1998
MODIFICATION TO SKVEKPATCH
General & Plastic Surgery
28d
Cleared
Dec 22, 1997
SYVEK PATCH
General & Plastic Surgery
137d