Zeltiq Aesthetics, Inc.
Zeltiq Aesthetics, Inc. holds FDA 510(k) medical device clearances, first cleared 2012, most recent 2024, with 6 FDA device recalls on record.
Top product codes for Zeltiq Aesthetics, Inc.
FDA recalls by Zeltiq Aesthetics, Inc.
- Z-1349-2022 — CoolCurve+ ZELTIQ Vacuum Applicator REF BRZ-AP1-064-000
- Z-1350-2022 — CoolFit ZELTIQ Vacuum Applicator REF BRZ-AP1-066-000
- Z-1348-2022 — CoolCurve ZELTIQ Vaccum Applicator REF BRZ-AP1-062-000
- Z-1346-2022 — CoolMax ZELTIQ Vacuum Applicator REF BRZ-AP1-080-000
- Z-1347-2022 — CoolCore ZELTIQ Vacuum Applicator REF BRZ-AP1-063-000
- Z-2383-2021 — CoolSculpting Elite System The CoolSculpting System SW release 2.0, SW release 3.0, SW release 3.0.1, SW release 3.0.2
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Zeltiq Aesthetics, Inc.
- K233804 — Resonic Rapid Acoustic Pulse Device
- K222629 — Resonic Rapid Acoustic Pulse Device
- K212707 — CoolSculpting Elite System
- K193566 — ZELTIQ CoolSculpting System
- K183514 — ZELTIQ CoolSculpting System
- K181740 — ZELTIQ CoolSculpting System
- K171069 — ZELTIQ CoolSculpting System
- K162050 — ZELTIQ CoolSculpting System
- K160259 — ZELTIQ CoolSculpting System
- K151179 — ZELTIQ CoolSculpting System
- K142491 — ZEL TIQ CoolSculpting System
- K133212 — ZELTIQ COOLSCULPTING SYSTEM
- K120023 — ZELTIQ COOLSCULPTING
Data sourced from openFDA. This site is unofficial and independent of the FDA.