Syneron Medical, Ltd. is one of 226 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Syneron Medical, Ltd. - FDA 510(k) Cleared Devices
35
Total
35
Cleared
0
Denied
Syneron Medical, Ltd. has 35 FDA 510(k) cleared general & plastic surgery devices. Based in Yokneam Elite, IL.
Historical record: 35 cleared submissions from 2002 to 2017.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Syneron Medical, Ltd.
35 devices
Cleared
May 15, 2017
ULTRASHAPE POWER SYSTEM
General & Plastic Surgery
98d
Cleared
Apr 20, 2017
SlimShape System
General & Plastic Surgery
136d
Cleared
Nov 17, 2016
UltraShape System
General & Plastic Surgery
107d
Cleared
Nov 07, 2016
UltraShape System
General & Plastic Surgery
115d
Cleared
Jul 08, 2016
ULTRASHAPE POWER SYSTEM
General & Plastic Surgery
99d
Cleared
Sep 15, 2015
CO2RE System
General & Plastic Surgery
89d
Cleared
Dec 08, 2014
TWO SKIN TREATMENT SYSTEM
General & Plastic Surgery
185d
Cleared
Oct 06, 2014
ULTRASHAPE SYSTEM
General & Plastic Surgery
104d
Cleared
Apr 10, 2014
CONTOUR I V3.1 SYSTEM
General & Plastic Surgery
171d
Cleared
Jul 19, 2013
TRANSCEND
General & Plastic Surgery
514d
Cleared
Oct 12, 2012
ME HAIR2GO
General & Plastic Surgery
134d
Cleared
Sep 13, 2012
VELASHAPE
General & Plastic Surgery
21d