Zeltiq Aesthetics, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Zeltiq Aesthetics, Inc. has 13 FDA 510(k) cleared general & plastic surgery devices. Based in Pleasanton, US.
Latest FDA clearance: Feb 2024. Active since 2012.
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.
13 devices
Cleared
Feb 01, 2024
Resonic Rapid Acoustic Pulse Device
General & Plastic Surgery
64d
Cleared
Sep 25, 2022
Resonic Rapid Acoustic Pulse Device
General & Plastic Surgery
25d
Cleared
Nov 05, 2021
CoolSculpting Elite System
General & Plastic Surgery
71d
Cleared
Jan 21, 2020
ZELTIQ CoolSculpting System
General & Plastic Surgery
29d
Cleared
Jan 14, 2019
ZELTIQ CoolSculpting System
General & Plastic Surgery
27d
Cleared
Aug 29, 2018
ZELTIQ CoolSculpting System
General & Plastic Surgery
58d
Cleared
Jul 07, 2017
ZELTIQ CoolSculpting System
General & Plastic Surgery
88d
Cleared
Nov 21, 2016
ZELTIQ CoolSculpting System
General & Plastic Surgery
119d
Cleared
Mar 23, 2016
ZELTIQ CoolSculpting System
General & Plastic Surgery
51d
Cleared
Sep 22, 2015
ZELTIQ CoolSculpting System
General & Plastic Surgery
141d
Cleared
Jan 26, 2015
ZEL TIQ CoolSculpting System
General & Plastic Surgery
144d
Cleared
Apr 09, 2014
ZELTIQ COOLSCULPTING SYSTEM
General & Plastic Surgery
173d