# Zeltiq Aesthetics, Inc.

- Location (FDA's records): Pleasanton, CA
- FDA decisions: 17 (2008–2024): 16 510(k) clearances and 1 De Novo grant
- Names in FDA's records: Zeltiq Aesthetics, Inc. (13); Zeltiq Aesthetics (4)
- Product codes: OOK (13), GEX (4)
- Predicates its devices cite: 24 (20 its own); citations of its devices by later devices: 27 (20 its own)
- Recalls linked to its devices: 6 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Juniper Medical, Inc.: 1 (https://510kreport.com/company/juniper-medical)
- Cynosure, Inc.: 1 (https://510kreport.com/company/cynosure)
- Spacelabs Medical, Inc.: 1 (https://510kreport.com/company/spacelabs-medical)
- Soliton, Inc.: 1 (https://510kreport.com/company/soliton)

## Firms that cite its devices most
- Cynosure, Inc.: 6 (https://510kreport.com/company/cynosure)
- Zeltiq Aesthetics, Inc. (Acquired by Allergan Aesthetics: 1 (https://510kreport.com/company/zeltiq-aesthetics-acquired-by-allergan-aesthetics)

## Its most-cited devices
- DEN090002: Zeltiq Aesthetics Dermal Cooling Device (2010), cited by 4
- K133212: Zeltiq Coolsculpting System (2014), cited by 4
- K120023: Zeltiq Coolsculpting (2012), cited by 3
- K162050: ZELTIQ CoolSculpting System (2016), cited by 3
- K151179: ZELTIQ CoolSculpting System (2015), cited by 2
- K172144: CoolSculpting System (2017), cited by 2

## Recent decisions
- K233804: Resonic Rapid Acoustic Pulse Device (Feb 1, 2024)
- K222629: Resonic Rapid Acoustic Pulse Device (Sep 25, 2022)
- K212707: CoolSculpting Elite System (Nov 5, 2021)
- K193566: ZELTIQ CoolSculpting System (Jan 21, 2020)
- K183514: ZELTIQ CoolSculpting System (Jan 14, 2019)
- K181740: ZELTIQ CoolSculpting System (Aug 29, 2018)
- K172144: CoolSculpting System (Nov 1, 2017)
- K171069: ZELTIQ CoolSculpting System (Jul 7, 2017)

Source page: https://510kreport.com/company/zeltiq-aesthetics