Erchonia Medical, Inc. is one of 4785 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Erchonia Medical, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Erchonia Medical, Inc. has 10 FDA 510(k) cleared medical devices. Based in Littleton, US.
Historical record: 10 cleared submissions from 2004 to 2016. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Erchonia Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Erchonia Medical, Inc.
10 devices
Cleared
Jun 03, 2016
LunulaLaser
General & Plastic Surgery
214d
Cleared
Apr 14, 2014
ERCHONIA ALLAY
Physical Medicine
207d
Cleared
Sep 16, 2013
ERCHONIA EMERGE
Physical Medicine
159d
Cleared
May 17, 2013
ERCHONIA VERJU LASER SYSTEM WITH MASSAGER
General & Plastic Surgery
44d
Cleared
Apr 23, 2013
ERCHONIA PL5000
Physical Medicine
35d
Cleared
May 14, 2012
MLS, ZERONA-AD
General & Plastic Surgery
108d
Cleared
Apr 24, 2008
ERCHONIA EML LASER
Physical Medicine
260d
Cleared
Mar 01, 2007
ERCHONIA IOTO_240
Physical Medicine
164d
Cleared
May 02, 2005
ERCHONIA EVRL LASER
General & Plastic Surgery
48d
Cleared
Sep 30, 2004
ERCHONIA EML LASER
Physical Medicine
153d