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.
FDA 510(k) cleared devices by Zeltiq Aesthetics, Inc.
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