510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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DEN090002Unknown

Zeltiq Aesthetics Dermal Cooling Device

Zeltiq Aesthetics Inc, Pleasanton CA / Post-NSE, Unknown
FDA source (opens on fda.gov)

DEN090002 is the FDA 510(k) clearance record for ZELTIQ AESTHETICS DERMAL COOLING DEVICE, a class II device, cleared for Zeltiq Aesthetics on under FDA product code OOK (Dermal Cooling Pack/Vacuum/Massager). FDA's definition for product code OOK reads: "The device is a combination of a cooling pad associated with a vacuum or mechanical massager intended for the disruption or induction of adipocyte cells indicated for body contouring or reduction in circumference of body areas". FDA records list 17 510(k) clearances for Zeltiq Aesthetics, from to . As of , FDA records show no recalls naming DEN090002.

Clearance record

Decision date
Received
(315 days to decision)
Product code
OOK Dermal Cooling Pack/Vacuum/Massager
Regulation
21 CFR 878.4340
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Zeltiq Aesthetics 4698 Willow Rd., Pleasanton CA
Third party review
No

Clearances, product code OOK

Trailing 12 months

FDA records hold no clearances under product code OOK in the trailing twelve months.

FDA records show no clearances under product code OOK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code OOK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260