Exciton Technologies, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Exciton Technologies, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mississauga, Ontario, CA.
Historical record: 7 cleared submissions from 2009 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Exciton Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Exciton Technologies, Inc.
7 devices
Cleared
Dec 06, 2018
KerraContact Ag Perf Advanced Perforated Silver Wound Dressing
General & Plastic Surgery
71d
Cleared
Feb 13, 2017
KerraCel Ag Gelling Fiber Silver Dressing
General & Plastic Surgery
158d
Cleared
Mar 26, 2014
EXSALT SD7 WOUND DRESSING WITH ADHESIVE BACKING
General & Plastic Surgery
104d
Cleared
Dec 15, 2011
EXSALT T7 WOUND DRESSING
General & Plastic Surgery
13d
Cleared
May 20, 2011
EXSALT SD7 WOUND DRESSING
General & Plastic Surgery
214d
Cleared
Oct 12, 2010
EXSALT WOUND DRESSING
General & Plastic Surgery
224d
Cleared
Jul 30, 2009
EXSALT SD7 WOUND DRESSING
General & Plastic Surgery
213d